A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458768



Internal ID22516651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16764793..16811766hg38UCSC Ensembl
chr10:16806792..16853765hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3846974
hg1946974
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855427
Supporting Variants
Samples
Known GenesRSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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