A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033378



Internal ID19122600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:57358610..57440466hg38UCSC Ensembl
Innerchr5:56654437..56736293hg19UCSC Ensembl
Innerchr5:56690194..56772050hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3881857
hg1981857
hg1881857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5672n100
Supporting Variantsnssv3642152
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)nsv1033378
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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