A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386488



Internal ID21044041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96863630..96869125hg38UCSC Ensembl
chr4:97784781..97790276hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg385496
hg195496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5378n223
Supporting Variantsnssv18121440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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