A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379948



Internal ID21037501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102163620..102177302hg38UCSC Ensembl
chr4:103084777..103098459hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3813683
hg1913683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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