A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969235



Internal ID22744170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19765343..19765343hg38UCSC Ensembl
chr19:19876152..19876152hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407213
Samples
Known GenesLINC00663
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969235
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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