A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452379



Internal ID22510252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18554812..18625262hg38UCSC Ensembl
chr10:18843741..18914191hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3870451
hg1970451
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860270
Supporting Variants
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452379
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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