A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117557



Internal ID21405552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61389837..61389837hg38UCSC Ensembl
chr20:59964893..59964893hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666744
Supporting Variants
SamplesHG00512
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117557
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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