A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604385



Internal ID16391794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103848379..103871334hg38UCSC Ensembl
Innerchr6:104296254..104319209hg19UCSC Ensembl
Innerchr6:104402947..104425902hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3822956
hg1922956
hg1822956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154856
Samples1780862404_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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