A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101722



Internal ID21454713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61518408..61521814hg38UCSC Ensembl
chr18:59185641..59189047hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383407
hg193407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584711
Supporting Variants
SamplesHG02011
Known GenesCDH20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101722
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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