A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981588



Internal ID18616785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138401895..138404533hg38UCSC Ensembl
Innerchr7:138086640..138089278hg19UCSC Ensembl
Innerchr7:137737180..137739818hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382639
hg192639
hg182639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2480227, nssv2480236, nssv2480234, nssv2480231, nssv2480233, nssv2480228, nssv2480232, nssv2480235, nssv2480230, nssv2480229
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)nsv981588
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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