A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374733



Internal ID21032286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15755646..15756244hg38UCSC Ensembl
chr4:15757269..15757867hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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