A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924538



Internal ID22699765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64732255..64732530hg38UCSC Ensembl
chr11:64499727..64500002hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367297
Samples
Known GenesRASGRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924538
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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