A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981537



Internal ID18616734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76472170..76506118hg38UCSC Ensembl
Innerchr7:76101487..76135435hg19UCSC Ensembl
Innerchr7:75939423..75973371hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3833949
hg1933949
hg1833949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2463841, nssv2463838, nssv2463840, nssv2463843, nssv2464636, nssv2463839, nssv2463842, nssv2464637, nssv2464638, nssv2463837
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDTX2, FDPSP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981537
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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