A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363892



Internal ID21021445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18895893..18896189hg38UCSC Ensembl
chr4:18897516..18897812hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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