A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290251



Internal ID20499469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154996962..154997094hg38UCSC Ensembl
chr1:154969438..154969570hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290251
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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