A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828041



Internal ID22602976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155222773..155235203hg38UCSC Ensembl
chr1:155192564..155204994hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3812431
hg1912431
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459580, nssv17453859, nssv17457703
Samples
Known GenesGBA, GBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828041
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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