A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2731086



Internal ID17760448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64407781..64412274hg38UCSC Ensembl
Innerchr9:43090842..43095332hg19UCSC Ensembl
Innerchr9:43080838..43085328hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384494
hg194491
hg184491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969570
Supporting Variants
SamplesHGDP00542
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2731086
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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