A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029503



Internal ID19118722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62323460..62988450hg38UCSC Ensembl
Innerchr6:63033365..63698355hg19UCSC Ensembl
Innerchr6:63091324..63756314hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38664991
hg19664991
hg18664991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657642
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)nsv1029503
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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