A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356696



Internal ID21014249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31291901..31293600hg38UCSC Ensembl
chr4:31293523..31295222hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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