A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532906



Internal ID20906267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38730266..38731735hg38UCSC Ensembl
chr19:39220906..39222375hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381470
hg191470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047818
Samples
Known GenesACTN4, CAPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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