A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394419



Internal ID21051972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100027863..100029299hg38UCSC Ensembl
chr4:100949020..100950456hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381437
hg191437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394419
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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