A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079255



Internal ID21449412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27008073..27009430hg38UCSC Ensembl
chr12:27161006..27162363hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg381358
hg191358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591727
Supporting Variants
SamplesHG00864
Known GenesTM7SF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079255
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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