A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906053



Internal ID4837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61386272..61386515hg38UCSC Ensembl
chr1:61851944..61852187hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420547
Supporting Variants
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906053
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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