A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381748



Internal ID21039301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100781296..100782703hg38UCSC Ensembl
chr4:101702453..101703860hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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