A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034487



Internal ID19123709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:118712108..118750230hg38UCSC Ensembl
Innerchr5:118047803..118085925hg19UCSC Ensembl
Innerchr5:118075702..118113824hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3838123
hg1938123
hg1838123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647232
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034487
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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