A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615496



Internal ID21807543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45175017..45176472hg38UCSC Ensembl
chr13:45749152..45750607hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036369
Supporting Variants
Samples
Known GenesGTF2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615496
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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