A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977713



Internal ID18612919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45319509..45328574hg38UCSC Ensembl
Innerchr15:45611707..45620772hg19UCSC Ensembl
Innerchr15:43398999..43408064hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg389066
hg199066
hg189066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2022150, nssv2022147, nssv2022146, nssv2022152, nssv2022153, nssv2022149, nssv2022154, nssv2022145, nssv2022148, nssv2022151
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)nsv977713
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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