A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380448



Internal ID21038001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10298018..10301811hg38UCSC Ensembl
chr5:10298130..10301923hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg383794
hg193794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122137
Samples
Known GenesCMBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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