A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711242



Internal ID21233003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55120514..55120514hg38UCSC Ensembl
chr8:56033074..56033074hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817753
Supporting Variants
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711242
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.046875


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