A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394484



Internal ID21052037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75675914..75757792hg38UCSC Ensembl
chr4:76601098..76678945hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3881879
hg1977848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120219
Samples
Known GenesUSO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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