A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058387



Internal ID15564887
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 StatusS
Merged Variantsnsv602953
Supporting Variants
Samples
Known GenesMTCH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058387
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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