A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902771



Internal ID2664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52204636..52210057hg38UCSC Ensembl
chr1:52670308..52675729hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385422
hg195422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419499
Supporting Variants
Samples
Known GenesZFYVE9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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