A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972761



Internal ID18607977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73645553..73651672hg38UCSC Ensembl
Innerchr9:76260469..76266588hg19UCSC Ensembl
Innerchr9:75450289..75456408hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386120
hg196120
hg186120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552932, nssv2552937, nssv2552936, nssv2552933, nssv2552934, nssv2552939, nssv2552931, nssv2552935, nssv2552940, nssv2552938
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972761
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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