A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974712



Internal ID18609923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62549229..62612165hg38UCSC Ensembl
Innerchr15:62841428..62904364hg19UCSC Ensembl
Innerchr15:60628720..60691656hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3862937
hg1962937
hg1862937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757451
SamplesHGDP01307
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974712
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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