A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033518



Internal ID19122739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78384340..78409480hg38UCSC Ensembl
Innerchr7:78013657..78038797hg19UCSC Ensembl
Innerchr7:77851593..77876733hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3825141
hg1925141
hg1825141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657118
Samples
Known GenesMAGI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033518
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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