A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982422



Internal ID18617617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64410068..64412274hg38UCSC Ensembl
Innerchr9:43090842..43093044hg19UCSC Ensembl
Innerchr9:43080838..43083040hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382207
hg192203
hg182203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731031, nssv2731024, nssv2731023, nssv2731027, nssv2731030, nssv2731025, nssv2731026, nssv2731029, nssv2731022, nssv2731028
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)nsv982422
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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