A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2031773



Internal ID17881770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74965193..74976489hg38UCSC Ensembl
Innerchr15:75257534..75268830hg19UCSC Ensembl
Innerchr15:73044587..73055883hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3811297
hg1911297
hg1811297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977735
Supporting Variants
SamplesHGDP01307
Known Genes
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)nssv2031773
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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