A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934500



Internal ID21354569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214864037..214866107hg38UCSC Ensembl
chr2:215728761..215730831hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177999
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934500
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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