A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374432



Internal ID22600101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4715616..4715695hg38UCSC Ensembl
chr17:4618911..4618990hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937264
Supporting Variants
Samples
Known GenesARRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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