A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2035239



Internal ID17501266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84117231..84429774hg38UCSC Ensembl
Innerchr15:84785983..84984473hg19UCSC Ensembl
Innerchr15:82576987..82775675hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38312544
hg19198491
hg18198689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976960
Supporting Variants
SamplesHGDP01029
Known GenesDNM1P41, EFTUD1P1, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
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)nssv2035239
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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