A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974594



Internal ID18609805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71054801..71064784hg38UCSC Ensembl
Innerchr15:71347140..71357123hg19UCSC Ensembl
Innerchr15:69134194..69144177hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg389984
hg199984
hg189984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2029179, nssv2029173, nssv2029180, nssv2029172, nssv2029177, nssv2029175, nssv2029176, nssv2029174, nssv2029178, nssv2029171
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)nsv974594
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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