A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966772



Internal ID18602002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32619107..32645287hg38UCSC Ensembl
Innerchr7:32658719..32684899hg19UCSC Ensembl
Innerchr7:32625244..32651424hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3826181
hg1926181
hg1826181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2441828, nssv2441821, nssv2441823, nssv2441829, nssv2441830, nssv2441822, nssv2441826, nssv2441825, nssv2441827, nssv2441824
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDPY19L1P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966772
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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