A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079148



Internal ID20646189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15621510..15621858hg38UCSC Ensembl
chr2:15761634..15761982hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341588
Supporting Variants
Samples
Known GenesDDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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