A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081396



Internal ID20648436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174704944..174757170hg38UCSC Ensembl
chr2:175569672..175621898hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3852227
hg1952227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350272
Supporting Variants
Samples
Known GenesCHRNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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