A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102500



Internal ID20669540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74006022..74006597hg38UCSC Ensembl
chr3:74055173..74055748hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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