A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268255



Internal ID20477473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26939070..26940997hg38UCSC Ensembl
chr1:27265561..27267488hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381928
hg191928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737856
Supporting Variants
Samples
Known GenesNUDC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268255
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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