A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977767



Internal ID18612973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101976499..101977746hg38UCSC Ensembl
Innerchr15:102516702..102517949hg19UCSC Ensembl
Innerchr15:100334225..100335472hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381248
hg191248
hg181248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2039368, nssv2627061, nssv2627056, nssv2627058, nssv2627060, nssv2039364, nssv2627063, nssv2039362, nssv2627059, nssv2039369, nssv2039370, nssv2627062, nssv2039365, nssv2039366, nssv2627057, nssv2039367, nssv2627064, nssv2039363, nssv2627055, nssv2039361
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDDX11L9, LOC100288778, WASH3P
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977767
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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