A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147957



Internal ID21510799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39096100..39096358hg38UCSC Ensembl
chr8:38953619..38953877hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576017
Supporting Variants
SamplesNA24385
Known GenesADAM9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147957
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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