A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094653



Internal ID21463240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97988613..97988739hg38UCSC Ensembl
chr12:98382391..98382517hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601392
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094653
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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