A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029701



Internal ID19118920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79175971..79226755hg38UCSC Ensembl
Innerchr7:78805287..78856071hg19UCSC Ensembl
Innerchr7:78643223..78694007hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3850785
hg1950785
hg1850785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6511n100
Supporting Variantsnssv3657168, nssv3657167
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)nsv1029701
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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