A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526402



Internal ID20899763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42633782..42769367hg38UCSC Ensembl
chr19:43137934..43273519hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38135586
hg19135586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046416
Samples
Known GenesLIPE-AS1, PSG3, PSG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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