A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122899



Internal ID20689939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117937401..117943200hg38UCSC Ensembl
chr5:117273096..117278895hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402532
Supporting Variants
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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