A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079256



Internal ID21502630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27062382..27062540hg38UCSC Ensembl
chr12:27215315..27215473hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587912
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079256
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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