A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029490



Internal ID19118709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4331007..4495166hg38UCSC Ensembl
Innerchr7:4370638..4534797hg19UCSC Ensembl
Innerchr7:4337164..4501323hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38164160
hg19164160
hg18164160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6233n100
Supporting Variantsnssv3655033
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)nsv1029490
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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