A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081341



Internal ID21475143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33470837..33471008hg38UCSC Ensembl
chr17:31797855..31798026hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603998
Supporting Variants
SamplesHG03371
Known GenesASIC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081341
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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