A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159866



Internal ID21407211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642009..121642064hg38UCSC Ensembl
chr9:124404288..124404343hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599457
Supporting Variants
SamplesHG00512
Known GenesDAB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159866
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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