A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030155



Internal ID19119374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29581537..29626117hg38UCSC Ensembl
Innerchr5:29581644..29626224hg19UCSC Ensembl
Innerchr5:29617401..29661981hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3844581
hg1944581
hg1844581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635999
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)nsv1030155
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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