A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624558



Internal ID21816605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29248441..29248553hg38UCSC Ensembl
chr17:27575459..27575571hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033528
Supporting Variants
Samples
Known GenesCRYBA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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