A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835187



Internal ID22610122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195172759..195173958hg38UCSC Ensembl
chr3:194893488..194894687hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489870, nssv17490101
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835187
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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