A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117568



Internal ID21472393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61406473..61406542hg38UCSC Ensembl
chr20:59981529..59981598hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586296
Supporting Variants
SamplesHG03125
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117568
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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