A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975412



Internal ID22750347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25678468..25678468hg38UCSC Ensembl
chr20:25659104..25659104hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402102
Samples
Known GenesZNF337
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975412
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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