A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600887



Internal ID21549530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61714214..61741658hg38UCSC Ensembl
chr20:60289270..60316714hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3827445
hg1927445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117369
SamplesNA20847
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600887
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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