A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910407



Internal ID22685618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77217772..77217873hg38UCSC Ensembl
chr11:76928817..76928918hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368910
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910407
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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