A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400140



Internal ID21057693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95846521..95853394hg38UCSC Ensembl
chr5:95182225..95189098hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg386874
hg196874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135617
Samples
Known GenesC5orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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