A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970951



Internal ID18606173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143085354..143095971hg38UCSC Ensembl
Innerchr7:142782447..142793064hg19UCSC Ensembl
Innerchr7:142492569..142503186hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810618
hg1910618
hg1810618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2482809, nssv2482808, nssv2482805, nssv2482807, nssv2482806, nssv2482811, nssv2482812, nssv2482810, nssv2482804, nssv2482803
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)nsv970951
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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