A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885407



Internal ID22660391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44025044..44028547hg38UCSC Ensembl
chr19:44529196..44532700hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg383504
hg193505
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476700
Samples
Known GenesZNF222
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885407
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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