A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445984



Internal ID21103537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113753401..113754400hg38UCSC Ensembl
chr10:115513160..115514159hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977666
Samples
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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