A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027880



Internal ID19117098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90479761..90537531hg38UCSC Ensembl
Innerchr7:90109075..90166845hg19UCSC Ensembl
Innerchr7:89947011..90004781hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3857771
hg1957771
hg1857771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6532n100
Supporting Variantsnssv3655234
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)nsv1027880
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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