A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2740712



Internal ID17883805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67890585..67891558hg38UCSC Ensembl
Innerchr9:67958031..67959004hg19UCSC Ensembl
Innerchr9:67547851..67548824hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982493
Supporting Variants
SamplesHGDP01307
Known GenesANKRD20A1, 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)nssv2740712
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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