A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2747372



Internal ID17883309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65810137..65830543hg38UCSC Ensembl
Innerchr9:70335502..70355908hg19UCSC Ensembl
Innerchr9:69575322..69595728hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820407
hg1920407
hg1820407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982535
Supporting Variants
SamplesHGDP01307
Known Genes
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)nssv2747372
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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