A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027497



Internal ID19116716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79172440..79226755hg38UCSC Ensembl
Innerchr7:78801756..78856071hg19UCSC Ensembl
Innerchr7:78639692..78694007hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3854316
hg1954316
hg1854316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6511n100
Supporting Variantsnssv3657120
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)nsv1027497
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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