A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453111



Internal ID21110664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112224493..112225261hg38UCSC Ensembl
chr9:114986773..114987541hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175246
Samples
Known GenesMIR3134, PTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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