A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041808



Internal ID20608848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4181993..4182418hg38UCSC Ensembl
chr18:4181993..4182418hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524026
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00136


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