A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086444



Internal ID21507242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11772152..11773839hg38UCSC Ensembl
chr16:11866008..11867695hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381688
hg191688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592536
Supporting Variants
SamplesNA19983
Known GenesZC3H7A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086444
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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