A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486524



Internal ID22544439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161101510..161112844hg38UCSC Ensembl
chr3:160819298..160830632hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3811335
hg1911335
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835058
Supporting Variants
Samples
Known GenesB3GALNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486524
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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