A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099570



Internal ID20666610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187069269..187070467hg38UCSC Ensembl
chr3:186787057..186788255hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356346
Supporting Variants
Samples
Known GenesST6GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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