A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901554



Internal ID1839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40480325..40480424hg38UCSC Ensembl
chr1:40945997..40946096hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424768
Supporting Variants
Samples
Known GenesZFP69
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901554
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008898


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