A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974602



Internal ID18609813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76471945..76473411hg38UCSC Ensembl
Innerchr15:76764286..76765752hg19UCSC Ensembl
Innerchr15:74551341..74552807hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381467
hg191467
hg181467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2032351, nssv2032345, nssv2032350, nssv2032344, nssv2032347, nssv2032352, nssv2032348, nssv2032346, nssv2032349, nssv2032353
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSCAPER
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974602
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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