A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026626



Internal ID19115844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54641954..54667163hg38UCSC Ensembl
Innerchr6:54506752..54531961hg19UCSC Ensembl
Innerchr6:54614711..54639920hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3825210
hg1925210
hg1825210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657485, nssv3657484, nssv3745493
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026626
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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