A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464397



Internal ID22522283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78472..81660hg38UCSC Ensembl
chr10:124412..127600hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383189
hg193189
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464397
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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