A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413856



Internal ID21071409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58495027..58495497hg38UCSC Ensembl
chr5:57790854..57791324hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133673
Samples
Known GenesGAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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