A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084060



Internal ID20651100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215766930..215767405hg38UCSC Ensembl
chr2:216631653..216632128hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352398
Supporting Variants
Samples
Known GenesLINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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