A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623300



Internal ID21815347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18249771..18250101hg38UCSC Ensembl
chr17:18153085..18153415hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025376
Supporting Variants
Samples
Known GenesFLII
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623300
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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