A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2731420



Internal ID17868967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65194067..65214345hg38UCSC Ensembl
Innerchr9:42788258..42808203hg19UCSC Ensembl
Innerchr9:42778254..42798199hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3820279
hg1919946
hg1819946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973606
Supporting Variants
SamplesHGDP01284
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)nssv2731420
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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