A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159266



Internal ID21402434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11313405..11313559hg38UCSC Ensembl
chr6:11313638..11313792hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572037
Supporting Variants
SamplesHG00171
Known GenesNEDD9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159266
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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