A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118508



Internal ID20685548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62087830..62098164hg38UCSC Ensembl
chr4:62953548..62963882hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3810335
hg1910335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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