A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388699



Internal ID21046252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144856630..144858002hg38UCSC Ensembl
chr4:145777782..145779154hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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