A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180664



Internal ID20747704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87082701..87093000hg38UCSC Ensembl
chr10:88842458..88852757hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438623
Supporting Variants
Samples
Known GenesGLUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180664
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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