A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2733877



Internal ID17817385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64412274..64417532hg38UCSC Ensembl
Innerchr9:43085586..43090842hg19UCSC Ensembl
Innerchr9:43075582..43080838hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385259
hg195257
hg185257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973263
Supporting Variants
SamplesHGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2733877
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