A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384795



Internal ID21042348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:117351839..117360812hg38UCSC Ensembl
chr4:118272995..118281968hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg388974
hg198974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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