A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373725



Internal ID21031278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28250624..28254364hg38UCSC Ensembl
chr4:28252246..28255986hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg383741
hg193741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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