A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495857



Internal ID272953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95101160..95102079hg38UCSC Ensembl
chr12:95494936..95495855hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684228
Samples
Known GenesFGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495857
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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