A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461977



Internal ID21119530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88436341..88775153hg38UCSC Ensembl
chr11:88169509..88508321hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38338813
hg19338813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189351
Samples
Known GenesGRM5, GRM5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461977
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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