A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020252



Internal ID19109471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158199878..158221090hg38UCSC Ensembl
Innerchr6:158620910..158642122hg19UCSC Ensembl
Innerchr6:158540898..158562110hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3821213
hg1921213
hg1821213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654489
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)nsv1020252
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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