A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259219



Internal ID20468437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31352236..31352236hg38UCSC Ensembl
chr1:31825083..31825083hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757487
Supporting Variants
Samples
Known GenesZCCHC17
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259219
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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