A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032586



Internal ID19121808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85868684..85916095hg38UCSC Ensembl
Innerchr5:85164502..85211913hg19UCSC Ensembl
Innerchr5:85200258..85247669hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3847412
hg1947412
hg1847412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639175
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)nsv1032586
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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