A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003067



Internal ID19092284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72284165..72323916hg38UCSC Ensembl
Innerchr1:72749848..72789599hg19UCSC Ensembl
Innerchr1:72522436..72562187hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3839752
hg1939752
hg1839752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv182n100
Supporting Variantsnssv3701260
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)nsv1003067
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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