A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970090



Internal ID18605314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27133130..27133723hg38UCSC Ensembl
Innerchr6:27100909..27101502hg19UCSC Ensembl
Innerchr6:27208888..27209481hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2399235, nssv2399232, nssv2399237, nssv2399238, nssv2399240, nssv2399234, nssv2399239, nssv2399231, nssv2399236, nssv2399233
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2AG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970090
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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