A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504853



Internal ID22562797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103546295..103559027hg38UCSC Ensembl
chr8:104558523..104571255hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3812733
hg1912733
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862173
Supporting Variants
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504853
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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