A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981564



Internal ID18616761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103064357..103072525hg38UCSC Ensembl
Innerchr7:102704804..102712972hg19UCSC Ensembl
Innerchr7:102492040..102500208hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388169
hg198169
hg188169
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2473525, nssv2473528, nssv2473531, nssv2473529, nssv2473530, nssv2473522, nssv2473523, nssv2473524, nssv2473526, nssv2473527
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFBXL13
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981564
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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