A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361694



Internal ID21019247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1515801..1518686hg38UCSC Ensembl
chr4:1517528..1520413hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382886
hg192886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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