A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2524250



Internal ID17469887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21141265..21142529hg38UCSC Ensembl
Innerchr9:21141264..21142528hg19UCSC Ensembl
Innerchr9:21131264..21132528hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381265
hg191265
hg181265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972299
Supporting Variants
SamplesHGDP00927
Known GenesIFNW1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2524250
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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