A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976943



Internal ID18612149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62267223..62274365hg38UCSC Ensembl
Innerchr15:62559422..62566564hg19UCSC Ensembl
Innerchr15:60346714..60353856hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg387143
hg197143
hg187143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2027535, nssv2027534, nssv2027537, nssv2027540, nssv2027539, nssv2027541, nssv2027538, nssv2027542, nssv2027533, nssv2027536
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976943
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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