A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2728476



Internal ID17760148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40252655..40254521hg38UCSC Ensembl
Innerchr9:42397673..42399539hg19UCSC Ensembl
Innerchr9:42387669..42389535hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg381867
hg191867
hg181867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973245
Supporting Variants
SamplesHGDP00521
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)nssv2728476
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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