A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528440



Internal ID20901801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1786554..1798674hg38UCSC Ensembl
chr19:1786553..1798673hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812121
hg1912121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045044
Samples
Known GenesATP8B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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