A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968662



Internal ID18603890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67721653..67742341hg38UCSC Ensembl
Innerchr9:46389835..46406699hg19UCSC Ensembl
Innerchr9:46279831..46296695hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3820689
hg1916865
hg1816865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2542941, nssv2542945, nssv2542940, nssv2542946, nssv2542947, nssv2542949, nssv2542944, nssv2542948, nssv2542943, nssv2542942
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968662
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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