A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475701



Internal ID21133254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101567383..101567824hg38UCSC Ensembl
chr13:102219734..102220175hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006302
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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