A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966766



Internal ID18601996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26922162..26924436hg38UCSC Ensembl
Innerchr7:26961781..26964055hg19UCSC Ensembl
Innerchr7:26928306..26930580hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382275
hg192275
hg182275
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2439418, nssv2439410, nssv2439413, nssv2439416, nssv2439411, nssv2439412, nssv2439417, nssv2439409, nssv2439415, nssv2439414
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966766
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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