A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496151



Internal ID22554084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87086110..87094581hg38UCSC Ensembl
chr3:87135260..87143731hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg388472
hg198472
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837422
Supporting Variants
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496151
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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