A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977734



Internal ID18612940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73161440..73163440hg38UCSC Ensembl
Innerchr15:73453781..73455781hg19UCSC Ensembl
Innerchr15:71240834..71242834hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382001
hg192001
hg182001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031639, nssv2031638, nssv2031644, nssv2031641, nssv2031647, nssv2031646, nssv2031640, nssv2031642, nssv2031643, nssv2031645
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNEO1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977734
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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