A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019541



Internal ID19108759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29786825..29814202hg38UCSC Ensembl
Innerchr5:29786932..29814309hg19UCSC Ensembl
Innerchr5:29822689..29850066hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3827378
hg1927378
hg1827378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5615n100
Supporting Variantsnssv3636018, nssv3636015, nssv3745865, nssv3636019, nssv3636017, nssv3745864, nssv3636020, nssv3636016, nssv3636021
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)nsv1019541
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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