A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153671



Internal ID15508738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29918387hg38UCSC Ensembl
Innerchr6:29859517..29886164hg19UCSC Ensembl
Innerchr6:29967496..29994143hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3826648
hg1926648
hg1826648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601314
Supporting Variants
Samples1780862590_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153671
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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