A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981617



Internal ID18616814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152820262..152820860hg38UCSC Ensembl
Innerchr7:152517347..152517945hg19UCSC Ensembl
Innerchr7:152148280..152148878hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38599
hg19599
hg18599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2489100, nssv2489104, nssv2489107, nssv2489109, nssv2489105, nssv2489102, nssv2489103, nssv2489101, nssv2489106, nssv2489108
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesACTR3B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981617
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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