A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14267201



Internal ID22203797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:61916667..61982986hg38UCSC Ensembl
Outerchr20:60491723..60558042hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3866320
hg1966320
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227101
Supporting Variants
SamplesHG00732
Known GenesCDH4, MIR1257, TAF4
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14267201
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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