A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051995



Internal ID20619035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153762901..153765400hg38UCSC Ensembl
chr1:153735377..153737876hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322486
Supporting Variants
Samples
Known GenesINTS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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