A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075963



Internal ID20643003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:121557394..121558047hg38UCSC Ensembl
chr2:122314970..122315623hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352745
Supporting Variants
Samples
Known GenesCLASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00679


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