A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052105



Internal ID20619145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155898501..155908900hg38UCSC Ensembl
chr1:155868292..155878691hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334694
Supporting Variants
Samples
Known GenesRIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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