A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523353



Internal ID20896714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47648937..47649239hg38UCSC Ensembl
chr19:48152194..48152496hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048308
Samples
Known GenesGLTSCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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