A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984105



Internal ID18619295
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 StatusM
Merged Variants
Supporting Variantsnssv2035643, nssv2035427, nssv2035641, nssv2035640, nssv2035644, nssv2035645, nssv2035642, nssv2035646, nssv2035426, nssv2035647
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00933, UBE2Q2P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984105
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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