A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356489



Internal ID21014042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20397444..20398010hg38UCSC Ensembl
chr4:20399067..20399633hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113239
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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