A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391751



Internal ID21049304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40633752..40635253hg38UCSC Ensembl
chr4:40635769..40637270hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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