A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077656



Internal ID21450267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122693937..122706672hg38UCSC Ensembl
chr12:123178484..123191219hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3812736
hg1912736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591613
Supporting Variants
SamplesHG01114
Known GenesHCAR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077656
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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