A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132943



Internal ID20699983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81992189..81992603hg38UCSC Ensembl
chr5:81288008..81288422hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404145
Supporting Variants
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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