A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057873



Internal ID15911059
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 StatusS
Merged Variantsnsv602864
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057873
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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