A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603694



Internal ID16044417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73565682..73656084hg38UCSC Ensembl
Innerchr6:74275405..74365807hg19UCSC Ensembl
Innerchr6:74332126..74422528hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3890403
hg1990403
hg1890403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1064037
Samples
Known GenesSLC17A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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