A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2744286



Internal ID17797852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64390347..64395677hg38UCSC Ensembl
Innerchr9:69402765..69408095hg19UCSC Ensembl
Innerchr9:68692585..68697915hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385331
hg195331
hg185331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969668
Supporting Variants
SamplesHGDP00778
Known GenesANKRD20A4
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)nssv2744286
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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