A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030774



Internal ID19119993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13735793..13783501hg38UCSC Ensembl
Innerchr6:13736025..13783733hg19UCSC Ensembl
Innerchr6:13844004..13891712hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3847709
hg1947709
hg1847709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749032
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)nsv1030774
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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