A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969550



Internal ID18604777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40261205..40263761hg38UCSC Ensembl
Innerchr9:42406223..42408779hg19UCSC Ensembl
Innerchr9:42396219..42398775hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382557
hg192557
hg182557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727989, nssv2727988, nssv2727992, nssv2727995, nssv2727990, nssv2727991, nssv2727993, nssv2727996, nssv2727987, nssv2727994
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969550
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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