A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487097



Internal ID22545012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168054021..168059567hg38UCSC Ensembl
chr3:167771809..167777355hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg385547
hg195547
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835367
Supporting Variants
Samples
Known GenesGOLIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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