A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087299



Internal ID21507030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96364894..96366309hg38UCSC Ensembl
chr14:96831231..96832646hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602878
Supporting Variants
SamplesNA19983
Known GenesGSKIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087299
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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