A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027422



Internal ID19116641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902717..9924385hg38UCSC Ensembl
Innerchr5:9902829..9924497hg19UCSC Ensembl
Innerchr5:9955829..9977497hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3821669
hg1921669
hg1821669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638190
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027422
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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