A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966756



Internal ID18601986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6801235..6805121hg38UCSC Ensembl
Innerchr7:6840866..6844752hg19UCSC Ensembl
Innerchr7:6807391..6811277hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg383887
hg193887
hg183887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2435225, nssv2435228, nssv2435224, nssv2435231, nssv2435227, nssv2435223, nssv2435226, nssv2435232, nssv2435229, nssv2435230
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCZ1B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966756
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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