A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391584



Internal ID21049137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10573197..10574808hg38UCSC Ensembl
chr5:10573309..10574920hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381612
hg191612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123994
Samples
Known GenesANKRD33B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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