A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884026



Internal ID22659008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210389084..210389172hg38UCSC Ensembl
chr1:210562428..210562516hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354395
Samples
Known GenesHHAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884026
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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