A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965702



Internal ID18600932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29790631..29831166hg38UCSC Ensembl
Innerchr6:29758408..29798943hg19UCSC Ensembl
Innerchr6:29866387..29906922hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3840536
hg1940536
hg1840536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2401695, nssv2401691, nssv2401697, nssv2401698, nssv2401693, nssv2401699, nssv2401694, nssv2401692, nssv2401690, nssv2401696
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHCG4, HLA-G, LOC554223
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965702
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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