A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016870



Internal ID19106087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7228529..7257261hg38UCSC Ensembl
Innerchr5:7228642..7257374hg19UCSC Ensembl
Innerchr5:7281642..7310374hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3828733
hg1928733
hg1828733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639634
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)nsv1016870
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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