A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450442



Internal ID21107995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131042201..131592500hg38UCSC Ensembl
chr10:132840464..133381404hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38550300
hg19540941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv913n223
Supporting Variantsnssv18187207
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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