A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468417



Internal ID21125970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62788502..62791876hg38UCSC Ensembl
chr11:62555974..62559348hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg383375
hg193375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993234
Samples
Known GenesMIR6748, TMEM179B, TMEM223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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