A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027037



Internal ID19116256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28936088..29147730hg38UCSC Ensembl
Innerchr5:28936195..29147837hg19UCSC Ensembl
Innerchr5:28971952..29183594hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38211643
hg19211643
hg18211643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5613n100
Supporting Variantsnssv3635980
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)nsv1027037
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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