A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602864



Internal ID16390273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34235629..34236755hg38UCSC Ensembl
Innerchr6:34203406..34204532hg19UCSC Ensembl
Innerchr6:34311384..34312510hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381127
hg191127
hg181127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1057873
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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