A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621988



Internal ID21814035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44387654..44387784hg38UCSC Ensembl
chr17:42465022..42465152hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029547
Supporting Variants
Samples
Known GenesITGA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621988
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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