A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087061



Internal ID21477652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19867766..19867987hg38UCSC Ensembl
chr17:19771079..19771300hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587028
Supporting Variants
SamplesHG03486
Known GenesULK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087061
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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