A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373565



Internal ID22599234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80231274..80231409hg38UCSC Ensembl
chr17:78205073..78205208hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936901
Supporting Variants
Samples
Known GenesSLC26A11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373565
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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