A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893316



Internal ID169700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180710498..180710648hg38UCSC Ensembl
chr1:180679634..180679784hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418132
Supporting Variants
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893316
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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