A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148685



Internal ID21495554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34618794..34618794hg38UCSC Ensembl
chr8:34476312..34476312hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635420
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148685
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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