A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262398



Internal ID20471616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6228420..6228489hg38UCSC Ensembl
chr1:6288480..6288549hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732114
Supporting Variants
Samples
Known GenesICMT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262398
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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