A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370362



Internal ID21027915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26568101..26573300hg38UCSC Ensembl
chr4:26569723..26574922hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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