A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596157



Internal ID20969228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35931905..35932091hg38UCSC Ensembl
chr20:34519827..34520013hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252534
Samples
Known GenesPHF20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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