A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480455



Internal ID21138008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44540102..44540808hg38UCSC Ensembl
chr13:45114238..45114944hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009131
Samples
Known GenesTSC22D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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