A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376768



Internal ID22602437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35280042..35373164hg38UCSC Ensembl
chr17:33607061..33700183hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3893123
hg1993123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928066
Supporting Variants
Samples
Known GenesSLFN11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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