A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2035643



Internal ID17728446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84536365..84594396hg38UCSC Ensembl
Innerchr15:85079596..85137627hg19UCSC Ensembl
Innerchr15:82880600..82938631hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3858032
hg1958032
hg1858032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984105
Supporting Variants
SamplesHGDP00456
Known GenesLINC00933, UBE2Q2P1
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)nssv2035643
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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