A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465571



Internal ID22523460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161669113..161675884hg38UCSC Ensembl
chr1:161638903..161645674hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg386772
hg196772
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828072
Supporting Variants
Samples
Known GenesFCGR2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465571
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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