A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470169



Internal ID21127722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128976836..128977529hg38UCSC Ensembl
chr11:128846731..128847424hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987542
Samples
Known GenesARHGAP32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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