A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2525614



Internal ID17835584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28145986..28150767hg38UCSC Ensembl
Innerchr9:28145984..28150765hg19UCSC Ensembl
Innerchr9:28135984..28140765hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg384782
hg194782
hg184782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968604
Supporting Variants
SamplesHGDP00998
Known GenesLINGO2
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)nssv2525614
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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