A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999560



Internal ID19159097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5218546..5266411hg38UCSC Ensembl
Innerchr1:5278606..5326471hg19UCSC Ensembl
Innerchr1:5178466..5226331hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3847866
hg1947866
hg1847866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3462759
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)nsv999560
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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