A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977693



Internal ID18266213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32388407..32403616hg38UCSC Ensembl
Innerchr15:32680608..32695817hg19UCSC Ensembl
Innerchr15:30467900..30483109hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3815210
hg1915210
hg1815210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2016709, nssv2016713, nssv2016706, nssv2016708, nssv2016714, nssv2016707, nssv2016711, nssv2016710, nssv2016712, nssv2016715
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesGOLGA8K
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977693
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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