A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970579



Internal ID18605801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131701487..131709971hg38UCSC Ensembl
Innerchr7:131386246..131394730hg19UCSC Ensembl
Innerchr7:131036786..131045270hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg388485
hg198485
hg188485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2476954, nssv2476959, nssv2476961, nssv2476962, nssv2476960, nssv2476957, nssv2476956, nssv2476955, nssv2476958, nssv2476963
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)nsv970579
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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