A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090027



Internal ID21469669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36923351..36923441hg38UCSC Ensembl
chr17:35280635..35280725hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599505
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090027
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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