A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2733313



Internal ID17808002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64387553..64390307hg38UCSC Ensembl
Innerchr9:43112789..43115543hg19UCSC Ensembl
Innerchr9:43102785..43105539hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382755
hg192755
hg182755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973619
Supporting Variants
SamplesHGDP00778
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)nssv2733313
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer