A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367800



Internal ID21025353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3816786..3827062hg38UCSC Ensembl
chr4:3818513..3828789hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3810277
hg1910277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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