A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052462



Internal ID20619502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160572648..160583539hg38UCSC Ensembl
chr1:160542438..160553329hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3810892
hg1910892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323497
Supporting Variants
Samples
Known GenesCD84
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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