A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972332



Internal ID18607548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42225841..42244659hg38UCSC Ensembl
Innerchr9:41266433..41285271hg19UCSC Ensembl
Innerchr9:41256433..41275271hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3818819
hg1918839
hg1818839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2534034, nssv2534036, nssv2534033, nssv2534035, nssv2534038, nssv2534032, nssv2534037, nssv2534040, nssv2534031, nssv2534039
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)nsv972332
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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