A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568219



Internal ID21760262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39822506..39822506hg38UCSC Ensembl
chr8:39680025..39680025hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062135
Supporting Variants
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568219
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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