A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473998



Internal ID21131551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128992412..128992925hg38UCSC Ensembl
chr11:128862307..128862820hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987544
Samples
Known GenesARHGAP32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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