A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378917



Internal ID21036470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44783846..44786410hg38UCSC Ensembl
chr4:44785863..44788427hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg382565
hg192565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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