A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055717



Internal ID15908903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32552380..32553041hg38UCSC Ensembl
Innerchr6:32520157..32520818hg19UCSC Ensembl
Innerchr6:32628135..32628796hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38662
hg19662
hg18662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602509
Supporting Variants
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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