A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090576



Internal ID21464090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51566491..51569500hg38UCSC Ensembl
chr12:51960275..51963284hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg383010
hg193010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586206
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090576
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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