A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127621



Internal ID20694661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164455733..164456179hg38UCSC Ensembl
chr5:163882739..163883185hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411591
Supporting Variants
Samples
Known GenesLOC101927835
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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