A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970882



Internal ID18606104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74973701..74974354hg38UCSC Ensembl
Innerchr7:74387851..74388504hg19UCSC Ensembl
Innerchr7:74025787..74026440hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38654
hg19654
hg18654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2719421, nssv2719420, nssv2719417, nssv2719424, nssv2719422, nssv2719419, nssv2719426, nssv2719418, nssv2719425, nssv2719423
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970882
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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