A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111647



Internal ID20678687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17173123..17175891hg38UCSC Ensembl
chr4:17174746..17177514hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg382769
hg192769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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