A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450075



Internal ID21107628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70855701..70865500hg38UCSC Ensembl
chr10:72615458..72625257hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185983
Samples
Known GenesSGPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450075
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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