A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604893



Internal ID16045616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068937..152070107hg38UCSC Ensembl
Innerchr6:152390072..152391242hg19UCSC Ensembl
Innerchr6:152431765..152432935hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381171
hg191171
hg181171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10971n54
Supporting Variantsnssv1074467
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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