A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057239



Internal ID20624279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209345386..209677728hg38UCSC Ensembl
chr1:209518731..209851073hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38332343
hg19332343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321267
Supporting Variants
Samples
Known GenesCAMK1G, G0S2, LAMB3, MIR205, MIR205HG, MIR4260
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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