A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937500



Internal ID21357570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239914639..239914751hg38UCSC Ensembl
chr2:240854056..240854168hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177851
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937500
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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