A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878226



Internal ID22653191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14488687..14490435hg38UCSC Ensembl
chr19:14599499..14601247hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381749
hg191749
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473227
Samples
Known GenesGIPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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