A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981669



Internal ID18616866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75316426..75325642hg38UCSC Ensembl
Innerchr7:74945596..74954835hg19UCSC Ensembl
Innerchr7:74783532..74792771hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389217
hg199240
hg189240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2720545, nssv2720547, nssv2720542, nssv2720540, nssv2720549, nssv2720548, nssv2720543, nssv2720546, nssv2720544, nssv2720541
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPMS2P5, SPDYE8P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981669
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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