A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603607



Internal ID16391016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68475768..68532128hg38UCSC Ensembl
Innerchr6:69185660..69242020hg19UCSC Ensembl
Innerchr6:69242381..69298741hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3856361
hg1956361
hg1856361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154806
Samples1780862076_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603607
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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