A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910526



Internal ID22685737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61122801..61123323hg38UCSC Ensembl
chr8:62035360..62035882hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910526
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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