A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023848



Internal ID19113065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84355712..84472458hg38UCSC Ensembl
Innerchr7:83985028..84101774hg19UCSC Ensembl
Innerchr7:83822964..83939710hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38116747
hg19116747
hg18116747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655161
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)nsv1023848
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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