A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530389



Internal ID20903750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18255492..18258505hg38UCSC Ensembl
chr19:18366302..18369315hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383014
hg193014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045079
Samples
Known GenesKIAA1683
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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