A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976952



Internal ID18612158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75415066..75419441hg38UCSC Ensembl
Innerchr15:75707407..75711782hg19UCSC Ensembl
Innerchr15:73494460..73498835hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384376
hg194376
hg184376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031123, nssv2031119, nssv2031122, nssv2031117, nssv2031118, nssv2031124, nssv2031120, nssv2031121, nssv2031116, nssv2031125
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSIN3A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976952
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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