A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015258



Internal ID19104475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:48639847..48746539hg38UCSC Ensembl
Innerchr6:48607583..48714176hg19UCSC Ensembl
Innerchr6:48715542..48822135hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38106693
hg19106594
hg18106594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5959n100
Supporting Variantsnssv3745481
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)nsv1015258
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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