A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905404



Internal ID4414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77883979..77885945hg38UCSC Ensembl
chr1:78349664..78351630hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381967
hg191967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138350
Supporting Variants
Samples
Known GenesNEXN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905404
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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