A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381780



Internal ID21039333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36806288..36827421hg38UCSC Ensembl
chr4:36807910..36829043hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3821134
hg1921134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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