A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127684



Internal ID20694724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156449175..156454966hg38UCSC Ensembl
chr5:155876185..155881976hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385792
hg195792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413522
Supporting Variants
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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