A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019355



Internal ID19108573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78690259..78770529hg38UCSC Ensembl
Innerchr7:78319575..78399845hg19UCSC Ensembl
Innerchr7:78157511..78237781hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3880271
hg1980271
hg1880271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755404
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)nsv1019355
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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