A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366337



Internal ID22592006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111889787..111912145hg38UCSC Ensembl
chr1:112432409..112454767hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3822359
hg1922359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882364
Supporting Variants
Samples
Known GenesKCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366337
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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