A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976950



Internal ID18265470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74595906..74599031hg38UCSC Ensembl
Innerchr15:74888247..74891372hg19UCSC Ensembl
Innerchr15:72675300..72678425hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383126
hg193126
hg183126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031742, nssv2031746, nssv2031741, nssv2031748, nssv2031740, nssv2031744, nssv2031743, nssv2031749, nssv2031747, nssv2031745
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARID3B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976950
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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