A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123881



Internal ID20690922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12339986..12405483hg38UCSC Ensembl
chr5:12340098..12405595hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3865498
hg1965498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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