A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024625



Internal ID19113842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109873290..110033459hg38UCSC Ensembl
Innerchr5:109208991..109369160hg19UCSC Ensembl
Innerchr5:109236890..109397059hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38160170
hg19160170
hg18160170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647008
Samples
Known GenesLOC100289673
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024625
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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