A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083429



Internal ID20650469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214645006..214645390hg38UCSC Ensembl
chr2:215509730..215510114hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00211


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