A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112672



Internal ID20679712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165773301..165775300hg38UCSC Ensembl
chr4:166694453..166696452hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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