A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025187



Internal ID19114405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99583453..99838183hg38UCSC Ensembl
Innerchr5:98919157..99173887hg19UCSC Ensembl
Innerchr5:98947056..99201786hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38254731
hg19254731
hg18254731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638068
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)nsv1025187
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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