A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437341



Internal ID22495211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39822506..39822506hg38UCSC Ensembl
chr8:39680025..39680025hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948678
Supporting Variants
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437341
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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