A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974586



Internal ID18609797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62360435..62362736hg38UCSC Ensembl
Innerchr15:62652634..62654935hg19UCSC Ensembl
Innerchr15:60439926..60442227hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382302
hg192302
hg182302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2027639, nssv2027630, nssv2027637, nssv2027632, nssv2027631, nssv2027636, nssv2027638, nssv2027633, nssv2027634, nssv2027635
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)nsv974586
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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