A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052519



Internal ID20619559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162700413..162700923hg38UCSC Ensembl
chr1:162670203..162670713hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330907
Supporting Variants
Samples
Known GenesDDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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