A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023501



Internal ID20590541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31063001..31099444hg38UCSC Ensembl
chr15:31355204..31391647hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3836444
hg1936444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512050
Supporting Variants
Samples
Known GenesMIR211, TRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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