A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981511



Internal ID18616708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66602389..66610934hg38UCSC Ensembl
Innerchr7:66067376..66075921hg19UCSC Ensembl
Innerchr7:65704811..65713356hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg388546
hg198546
hg188546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2459619, nssv2460153, nssv2460152, nssv2459617, nssv2460148, nssv2460149, nssv2459618, nssv2460151, nssv2459616, nssv2460150
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)nsv981511
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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