A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2745720



Internal ID17874914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64406715..64407350hg38UCSC Ensembl
Innerchr9:69419133..69419768hg19UCSC Ensembl
Innerchr9:68708953..68709588hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38636
hg19636
hg18636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969670
Supporting Variants
SamplesHGDP01284
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)nssv2745720
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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