A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970812



Internal ID18606034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34869091..34897630hg38UCSC Ensembl
Innerchr7:34908703..34937242hg19UCSC Ensembl
Innerchr7:34875228..34903767hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3828540
hg1928540
hg1828540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2440391, nssv2440399, nssv2440397, nssv2440394, nssv2440390, nssv2440395, nssv2440393, nssv2440396, nssv2440398, nssv2440392
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNPSR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970812
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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