A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835184



Internal ID22610119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195092944..195128678hg38UCSC Ensembl
chr3:194813673..194849407hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3835735
hg1935735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489867
Samples
Known GenesXXYLT1, XXYLT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835184
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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