A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966777



Internal ID18255321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35841798..35866093hg38UCSC Ensembl
Innerchr7:35881408..35905703hg19UCSC Ensembl
Innerchr7:35847933..35872228hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3824296
hg1924296
hg1824296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2443119, nssv2443127, nssv2443123, nssv2443118, nssv2443126, nssv2443125, nssv2443122, nssv2443124, nssv2443120, nssv2443121
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesSEPT7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966777
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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