A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18130799



Internal ID20697839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39519102..39524638hg38UCSC Ensembl
chr5:39519204..39524740hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg385537
hg195537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381382
Supporting Variants
Samples
Known GenesLOC101926940
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18130799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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