A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395043



Internal ID21052596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169912388..169912754hg38UCSC Ensembl
chr4:170833539..170833905hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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