A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2722985



Internal ID17773597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33572281..33576350hg38UCSC Ensembl
Innerchr9:33572279..33576348hg19UCSC Ensembl
Innerchr9:33562279..33566348hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384070
hg194070
hg184070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973207
Supporting Variants
SamplesHGDP00542
Known GenesANKRD18B
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)nssv2722985
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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