A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977756



Internal ID18266276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89687413..89689672hg38UCSC Ensembl
Innerchr15:90230644..90232903hg19UCSC Ensembl
Innerchr15:88031648..88033907hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382260
hg192260
hg182260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2037417, nssv2037414, nssv2037415, nssv2037419, nssv2037418, nssv2037416, nssv2037413, nssv2037412, nssv2037421, nssv2037420
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesPEX11A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977756
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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