A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156224



Internal ID21441129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108900756..108900840hg38UCSC Ensembl
chr9:111663036..111663120hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590576
Supporting Variants
SamplesHG00732
Known GenesIKBKAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156224
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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