A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400020



Internal ID21057573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116196255..116275004hg38UCSC Ensembl
chr5:115531952..115610701hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3878750
hg1978750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125684
Samples
Known GenesCOMMD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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