A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452084



Internal ID21109637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4179320..4183295hg38UCSC Ensembl
chr10:4221512..4225487hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383976
hg193976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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