A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966864



Internal ID18602093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98477206..98479434hg38UCSC Ensembl
Innerchr7:98106518..98108746hg19UCSC Ensembl
Innerchr7:97944454..97946682hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382229
hg192229
hg182229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470629, nssv2470633, nssv2470638, nssv2470631, nssv2470630, nssv2470632, nssv2470637, nssv2470635, nssv2470634, nssv2470636
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)nsv966864
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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