A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963952



Internal ID18252504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:111125682..111135485hg38UCSC Ensembl
Innerchr2:111883259..111893062hg19UCSC Ensembl
Innerchr2:111599730..111609533hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg389804
hg199804
hg189804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758540
SamplesHGDP00778
Known GenesBCL2L11
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963952
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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