A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366936



Internal ID21024489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28913477..28914145hg38UCSC Ensembl
chr4:28915099..28915767hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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