A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492616



Internal ID22550544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48081123..48082166hg38UCSC Ensembl
chr3:48122613..48123656hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381044
hg191044
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836348
Supporting Variants
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492616
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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