A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835513



Internal ID22610448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195186808..195188107hg38UCSC Ensembl
chr3:194907537..194908836hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489871, nssv17489872
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835513
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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