A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020779



Internal ID19109997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7457084..7495981hg38UCSC Ensembl
Innerchr5:7457197..7496094hg19UCSC Ensembl
Innerchr5:7510197..7549094hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3838898
hg1938898
hg1838898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639645
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020779
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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