A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034274



Internal ID19123496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109363517..109440339hg38UCSC Ensembl
Innerchr7:109003574..109080396hg19UCSC Ensembl
Innerchr7:108790810..108867632hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3876823
hg1976823
hg1876823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656231
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)nsv1034274
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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