A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107042



Internal ID20674082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106142387..106148384hg38UCSC Ensembl
chr4:107063544..107069541hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384700
Supporting Variants
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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