A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974608



Internal ID18609819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79742169..79744968hg38UCSC Ensembl
Innerchr15:80034511..80037310hg19UCSC Ensembl
Innerchr15:77821566..77824365hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382800
hg192800
hg182800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2033230, nssv2033231, nssv2033235, nssv2033233, nssv2033229, nssv2033228, nssv2033237, nssv2033232, nssv2033234, nssv2033236
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)nsv974608
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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