A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970816



Internal ID18259352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35903117..35905406hg38UCSC Ensembl
Innerchr7:35942727..35945016hg19UCSC Ensembl
Innerchr7:35909252..35911541hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg382290
hg192290
hg182290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2443313, nssv2444111, nssv2443315, nssv2444108, nssv2444112, nssv2443314, nssv2444110, nssv2444109, nssv2443312, nssv2444113
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSEPT7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970816
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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