A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102835



Internal ID20669875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56554958..56557258hg38UCSC Ensembl
chr3:56588986..56591286hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359025
Supporting Variants
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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