A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475969



Internal ID21133522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57635201..57672300hg38UCSC Ensembl
chr13:58209335..58246434hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3837100
hg1937100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1855n223
Supporting Variantsnssv18178611
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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