A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530188



Internal ID21854544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85767569..85767569hg38UCSC Ensembl
chr2:85994692..85994692hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050383
Supporting Variants
Samples
Known GenesATOH8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530188
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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