A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107634



Internal ID20674675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106358001..106360000hg38UCSC Ensembl
chr4:107279158..107281157hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381620
Supporting Variants
Samples
Known GenesGIMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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