A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464338



Internal ID22522224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9730557..9753352hg38UCSC Ensembl
chr10:9772520..9795315hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3822796
hg1922796
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464338
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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