A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450143



Internal ID22508013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8654356..8657942hg38UCSC Ensembl
chr10:8696319..8699905hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383587
hg193587
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450143
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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