A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061007



Internal ID19150226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15102422..15249168hg38UCSC Ensembl
Innerchr18:15102421..15249167hg19UCSC Ensembl
Innerchr18:15092421..15239167hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38146747
hg19146747
hg18146747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725297
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)nsv1061007
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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