A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953754



Internal ID17302628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:20558041..20574140hg38UCSC Ensembl
Outerchr2:20757801..20773900hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3816100
hg1916100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001694
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953754
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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