A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665957



Internal ID15055923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38503356..38542187hg38UCSC Ensembl
Innerchr5:38503458..38542289hg19UCSC Ensembl
Innerchr5:38539215..38578046hg18UCSC Ensembl
Innerchr5:38539215..38578046hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3838832
hg1938832
hg1838832
hg1738832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516065
Supporting Variants
Samples
Known GenesLIFR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665957
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer