A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970453



Internal ID18258989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25122317..25124488hg38UCSC Ensembl
Innerchr7:25161936..25164107hg19UCSC Ensembl
Innerchr7:25128461..25130632hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382172
hg192172
hg182172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438559, nssv2438556, nssv2438560, nssv2438552, nssv2438557, nssv2438551, nssv2438553, nssv2438554, nssv2438555, nssv2438558
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCYCS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970453
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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