A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378801



Internal ID21036354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109563875..109577095hg38UCSC Ensembl
chr4:110485031..110498251hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3813221
hg1913221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107762
Samples
Known GenesCCDC109B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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