A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356756



Internal ID21014309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8169463..8174871hg38UCSC Ensembl
chr4:8171190..8176598hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg385409
hg195409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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