A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087606



Internal ID20654646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55741801..55793600hg38UCSC Ensembl
chr2:55968936..56020735hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3851800
hg1951800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343727
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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