A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117736



Internal ID20684776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5526758..5530718hg38UCSC Ensembl
chr4:5528485..5532445hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg383961
hg193961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356869
Supporting Variants
Samples
Known GenesC4orf6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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