A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086810



Internal ID21459157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74801385..74801473hg38UCSC Ensembl
chr17:72797524..72797612hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586819
Supporting Variants
SamplesHG02818
Known GenesTMEM104
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086810
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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