A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456086



Internal ID22513963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149780277..149816483hg38UCSC Ensembl
chr1:149751833..149788037hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3836207
hg1936205
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828343
Supporting Variants
Samples
Known GenesFCGR1A, HIST2H2BF, HIST2H3D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456086
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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