A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982243



Internal ID18617438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64342429..64501598hg38UCSC Ensembl
Innerchr9:42995364..43160734hg19UCSC Ensembl
Innerchr9:42985360..43150730hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38159170
hg19165371
hg18165371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2538094, nssv2538093, nssv2538091, nssv2538096, nssv2538090, nssv2538099, nssv2538098, nssv2538092, nssv2538095, nssv2538097
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3, FAM95B1, LOC642929
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982243
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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