A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459689



Internal ID22517575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96845480..96862646hg38UCSC Ensembl
chr10:98605237..98622403hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3817167
hg1917167
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855749
Supporting Variants
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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