A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052035



Internal ID102538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93162431..93205597hg38UCSC Ensembl
chr11:92895597..92938763hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3843167
hg1943167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510149
Supporting Variants
Samples
Known GenesSLC36A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052035
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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