A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2728277



Internal ID17755495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40244197..40244697hg38UCSC Ensembl
Innerchr9:42389215..42389715hg19UCSC Ensembl
Innerchr9:42379211..42379711hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982397
Supporting Variants
SamplesHGDP00521
Known GenesANKRD20A2, ANKRD20A3
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)nssv2728277
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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