A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970881



Internal ID18606103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73400883..73411186hg38UCSC Ensembl
Innerchr7:72815213..72825516hg19UCSC Ensembl
Innerchr7:72453149..72463452hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3810304
hg1910304
hg1810304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2463392, nssv2463391, nssv2463397, nssv2463398, nssv2463394, nssv2463399, nssv2463400, nssv2463396, nssv2463395, nssv2463393
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)nsv970881
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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