A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051733



Internal ID15558233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29865764..29901207hg38UCSC Ensembl
Innerchr6:29833541..29868984hg19UCSC Ensembl
Innerchr6:29941520..29976963hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3835444
hg1935444
hg1835444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601241
Supporting Variants
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051733
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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