A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448977



Internal ID21106530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99900254..99900770hg38UCSC Ensembl
chr10:101660011..101660527hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192688
Samples
Known GenesDNMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448977
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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