A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132083



Internal ID20699123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64413048..64477399hg38UCSC Ensembl
chr5:63708875..63773226hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3864352
hg1964352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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