A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133259



Internal ID20700299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65932075..65941997hg38UCSC Ensembl
chr5:65227903..65237825hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg389923
hg199923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413227
Supporting Variants
Samples
Known GenesERBB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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