A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495078



Internal ID21152631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113452165..113453859hg38UCSC Ensembl
chr13:114106480..114108174hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007759
Samples
Known GenesADPRHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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