A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450823



Internal ID21108376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37768366..37899580hg38UCSC Ensembl
chr10:38057294..38188508hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38131215
hg19131215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194091
Samples
Known GenesZNF248, ZNF33BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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