A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604899



Internal ID16392308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068937..152071039hg38UCSC Ensembl
Innerchr6:152390072..152392174hg19UCSC Ensembl
Innerchr6:152431765..152433867hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10970n54
Supporting Variantsnssv1074554, nssv1074541, nssv1074559, nssv1074558, nssv1074507, nssv1074562, nssv1074564, nssv1074532, nssv1074518, nssv1074531, nssv1074508, nssv1074512, nssv1074543, nssv1074514, nssv1074524, nssv1074523, nssv1074556, nssv1074535, nssv1074563, nssv1074542, nssv1074498, nssv1074515, nssv1074516, nssv1074536, nssv1074555, nssv1074528, nssv1074520, nssv1074552, nssv1074540, nssv1074561, nssv1074537, nssv1074550, nssv1074511, nssv1074548, nssv1074519, nssv1074560, nssv1074510, nssv1074500, nssv1074530, nssv1074517, nssv1074547, nssv1074529, nssv1074509, nssv1074522, nssv1074526, nssv1074513, nssv1074505, nssv1074503, nssv1074501, nssv1074499, nssv1074533, nssv1074525, nssv1074534, nssv1074502, nssv1074551, nssv1074546, nssv1074506, nssv1074553, nssv1074544, nssv1074527, nssv1074521, nssv1074549, nssv1074538, nssv1074545, nssv1074504, nssv1074539, nssv1074557
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604899
Frequency
Sample Size17421
Observed Gain0
Observed Loss67
Observed Complex0
Frequencyn/a


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