A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585518



Internal ID21777561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61658855..61658855hg38UCSC Ensembl
chr8:62571414..62571414hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075937
Supporting Variants
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585518
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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