A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976917



Internal ID18265437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33012332..33013720hg38UCSC Ensembl
Innerchr15:33304533..33305921hg19UCSC Ensembl
Innerchr15:31091825..31093213hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381389
hg191389
hg181389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2018381, nssv2018377, nssv2018378, nssv2018380, nssv2018384, nssv2018382, nssv2018379, nssv2018383, nssv2018385, nssv2018376
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFMN1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976917
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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