A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147808



Internal ID21451500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39045006..39045006hg38UCSC Ensembl
chr8:38902525..38902525hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630189
Supporting Variants
SamplesHG01505
Known GenesADAM9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147808
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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