A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027068



Internal ID19116287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66436556..66526224hg38UCSC Ensembl
Innerchr7:65901543..65991211hg19UCSC Ensembl
Innerchr7:65538978..65628646hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3889669
hg1989669
hg1889669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755292
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)nsv1027068
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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