A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034897



Internal ID18777429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114133022..114234515hg38UCSC Ensembl
Innerchr6:114454186..114555679hg19UCSC Ensembl
Innerchr6:114560879..114662372hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38101494
hg19101494
hg18101494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6139n100
Supporting Variantsnssv3654308
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)nsv1034897
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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