A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974616



Internal ID18609827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84940250..84943490hg38UCSC Ensembl
Innerchr15:85483481..85486721hg19UCSC Ensembl
Innerchr15:83284485..83287725hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383241
hg193241
hg183241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2035738, nssv2035739, nssv2035735, nssv2035741, nssv2035737, nssv2035742, nssv2035736, nssv2035744, nssv2035743, nssv2035740
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSLC28A1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974616
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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