A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116948



Internal ID20683988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36064401..36065800hg38UCSC Ensembl
chr4:36066023..36067422hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364694
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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