A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517150



Internal ID20890511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38647301..38647900hg38UCSC Ensembl
chr19:39137941..39138540hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047811
Samples
Known GenesACTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517150
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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