A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2722947



Internal ID17806644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33566606..33567344hg38UCSC Ensembl
Innerchr9:33566604..33567342hg19UCSC Ensembl
Innerchr9:33556604..33557342hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38739
hg19739
hg18739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973205
Supporting Variants
SamplesHGDP00778
Known GenesANKRD18B
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2722947
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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