A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607372



Internal ID21799419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102633356..102633356hg38UCSC Ensembl
chr14:103099693..103099693hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084032
Supporting Variants
Samples
Known GenesRCOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607372
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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