A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032357



Internal ID19121579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79175971..79227321hg38UCSC Ensembl
Innerchr7:78805287..78856637hg19UCSC Ensembl
Innerchr7:78643223..78694573hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3851351
hg1951351
hg1851351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6511n100
Supporting Variantsnssv3657169
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)nsv1032357
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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