A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023379



Internal ID19112596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109363517..109715177hg38UCSC Ensembl
Innerchr7:109003574..109355234hg19UCSC Ensembl
Innerchr7:108790810..109142470hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38351661
hg19351661
hg18351661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755482
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)nsv1023379
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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