A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965162



Internal ID18600396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44577610..44581731hg38UCSC Ensembl
Innerchr3:44619102..44623223hg19UCSC Ensembl
Innerchr3:44594106..44598227hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384122
hg194122
hg184122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2279504, nssv2279508, nssv2279503, nssv2279506, nssv2279501, nssv2279507, nssv2279502, nssv2279509, nssv2279505, nssv2279500
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZKSCAN7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965162
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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