A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027950



Internal ID18770481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:157796915..157824894hg38UCSC Ensembl
Innerchr5:157223923..157251902hg19UCSC Ensembl
Innerchr5:157156501..157184480hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3827980
hg1927980
hg1827980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648221
Samples
Known GenesCLINT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027950
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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