A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414921



Internal ID21072474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52930702..52931225hg38UCSC Ensembl
chr5:52226532..52227055hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132323
Samples
Known GenesITGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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