A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2727687



Internal ID17730989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40247551..40249430hg38UCSC Ensembl
Innerchr9:42392569..42394448hg19UCSC Ensembl
Innerchr9:42382565..42384444hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg381880
hg191880
hg181880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973244
Supporting Variants
SamplesHGDP00456
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)nssv2727687
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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