A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981351



Internal ID18616549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32484334..32518729hg38UCSC Ensembl
Innerchr6:32452111..32486506hg19UCSC Ensembl
Innerchr6:32560089..32594484hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3834396
hg1934396
hg1834396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758260, nssv2764024, nssv2764973, nssv2759362, nssv2757037, nssv2757067
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00542, HGDP00927
Known GenesHLA-DRB5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981351
Frequency
Sample Size10
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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