A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077641



Internal ID21468999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121958626..121958705hg38UCSC Ensembl
chr12:122396532..122396611hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592824
Supporting Variants
SamplesHG03125
Known GenesWDR66
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077641
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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