A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060160



Internal ID20627200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24744514..24747258hg38UCSC Ensembl
chr1:25071005..25073749hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382745
hg192745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321044
Supporting Variants
Samples
Known GenesCLIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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