A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3701259



Internal ID18999540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72284165..72313579hg38UCSC Ensembl
Innerchr1:72749848..72779262hg19UCSC Ensembl
Innerchr1:72522436..72551850hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3829415
hg1929415
hg1829415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005892
Supporting Variants
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)nssv3701259
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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