A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031787



Internal ID19121009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62563335..62660746hg38UCSC Ensembl
Innerchr6:63273240..63370651hg19UCSC Ensembl
Innerchr6:63331199..63428610hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3897412
hg1997412
hg1897412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657644
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)nsv1031787
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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