A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442134



Internal ID21099687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113355625..113376198hg38UCSC Ensembl
chr9:116117905..116138478hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3820574
hg1920574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229384
Samples
Known GenesBSPRY, HDHD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442134
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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