A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478279



Internal ID21135832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101448301..101456200hg38UCSC Ensembl
chr13:102100652..102108551hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196008
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478279
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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