A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275610



Internal ID20484828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55120523..55120523hg38UCSC Ensembl
chr8:56033083..56033083hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751570
Supporting Variants
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275610
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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