A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697208



Internal ID15087174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146655993..146671213hg38UCSC Ensembl
Innerchr5:146035556..146050776hg19UCSC Ensembl
Innerchr5:146015749..146030969hg18UCSC Ensembl
Innerchr5:146015749..146030969hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3815221
hg1915221
hg1815221
hg1715221
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520071
Supporting Variants
Samples
Known GenesPPP2R2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697208
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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