A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602726



Internal ID16390135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32641349..32658151hg38UCSC Ensembl
Innerchr6:32609126..32625928hg19UCSC Ensembl
Innerchr6:32717104..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3816803
hg1916803
hg1816803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10591n54
Supporting Variantsnssv1056555, nssv1056570, nssv1056557, nssv1056569, nssv1056576, nssv1056563, nssv1056581, nssv1056574, nssv1056571, nssv1056567, nssv1056568, nssv1056572, nssv1056577, nssv1056560, nssv1056579, nssv1056578, nssv1056558, nssv1056583, nssv1056580, nssv1056554, nssv1056573, nssv1056565, nssv1056566, nssv1056556, nssv1056559, nssv1056561, nssv1056553, nssv1056575, nssv1056562, nssv1056564, nssv1056582, nssv1056552
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602726
Frequency
Sample Size17421
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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