A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412541



Internal ID21070094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148775488..148776368hg38UCSC Ensembl
chr5:148155051..148155931hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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