A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067047



Internal ID19156266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76271051..76339603hg38UCSC Ensembl
Innerchr18:73983006..74051558hg19UCSC Ensembl
Innerchr18:72111994..72180546hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3868553
hg1968553
hg1868553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563029
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)nsv1067047
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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