A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101077



Internal ID21493255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24023933..24023982hg38UCSC Ensembl
chr18:21603897..21603946hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587599
Supporting Variants
SamplesNA19238
Known GenesTTC39C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101077
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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