A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107288



Internal ID20674328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135912412..135913135hg38UCSC Ensembl
chr4:136833567..136834290hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384997
Supporting Variants
Samples
Known GenesLINC00613
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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