A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077646



Internal ID21415295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122124331..122124413hg38UCSC Ensembl
chr12:122608878..122608960hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586617
Supporting Variants
SamplesHG00731
Known GenesMLXIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077646
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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