A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450394



Internal ID21107947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23092601..23100300hg38UCSC Ensembl
chr10:23381530..23389229hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv651n223
Supporting Variantsnssv18187439
Samples
Known GenesMSRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450394
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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