A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359194



Internal ID21016747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48825130..48835506hg38UCSC Ensembl
chr3:48862563..48872939hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3810377
hg1910377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101998
Samples
Known GenesPRKAR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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