A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109643



Internal ID20676683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148225204..148225613hg38UCSC Ensembl
chr4:149146356..149146765hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377844
Supporting Variants
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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