A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901556



Internal ID1840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40484420..40484451hg38UCSC Ensembl
chr1:40950092..40950123hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550977
Supporting Variants
Samples
Known GenesZFP69
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901556
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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