A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091018



Internal ID20658058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7958801..7960700hg38UCSC Ensembl
chr2:8098932..8100831hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353742
Supporting Variants
Samples
Known GenesLINC00298
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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