A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397746



Internal ID21055299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124803817..124804053hg38UCSC Ensembl
chr5:124139510..124139746hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397746
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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