A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453414



Internal ID21110967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100180801..100190000hg38UCSC Ensembl
chr10:101940558..101949757hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184195
Samples
Known GenesCHUK, ERLIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453414
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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