A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704171



Internal ID15094137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160405901..160411656hg38UCSC Ensembl
Innerchr5:159832908..159838663hg19UCSC Ensembl
Innerchr5:159765486..159771241hg18UCSC Ensembl
Innerchr5:159765486..159771241hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385756
hg195756
hg185756
hg175756
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527693
Supporting Variants
Samples
Known GenesSLU7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704171
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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