A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602953



Internal ID16043676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36985315..36986306hg38UCSC Ensembl
Innerchr6:36953091..36954082hg19UCSC Ensembl
Innerchr6:37061069..37062060hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38992
hg19992
hg18992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058387
Samples
Known GenesMTCH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602953
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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