A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970363



Internal ID18258900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31382550..31486386hg38UCSC Ensembl
Innerchr6:31350327..31454163hg19UCSC Ensembl
Innerchr6:31458306..31562142hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38103837
hg19103837
hg18103837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759367, nssv2758820, nssv2765012, nssv2765665, nssv2757935, nssv2765084, nssv2759366, nssv2757061, nssv2758878
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456
Known GenesHCG26, HCP5, MICA
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970363
Frequency
Sample Size10
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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