A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375779



Internal ID22601448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73063228..73078256hg38UCSC Ensembl
chr17:71059367..71074395hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3815029
hg1915029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934384
Supporting Variants
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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