A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984029



Internal ID18619219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25093662..25094162hg38UCSC Ensembl
Innerchr15:25338809..25339309hg19UCSC Ensembl
Innerchr15:22889902..22890402hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2012133, nssv2012138, nssv2012130, nssv2012132, nssv2012135, nssv2012129, nssv2012134, nssv2012131, nssv2012136, nssv2012137
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSNORD116-24
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984029
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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