A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489867



Internal ID22547788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195092944..195128678hg38UCSC Ensembl
chr3:194813673..194849407hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3835735
hg1935735
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835184
Supporting Variants
Samples
Known GenesXXYLT1, XXYLT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489867
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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