A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269115



Internal ID20478333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236038679..236038850hg38UCSC Ensembl
chr1:236201979..236202150hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746056
Supporting Variants
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269115
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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