A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607656



Internal ID16395065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78640059..78672103hg38UCSC Ensembl
Innerchr7:78269375..78301419hg19UCSC Ensembl
Innerchr7:78107311..78139355hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3832045
hg1932045
hg1832045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1088517
Samples
Known GenesMAGI2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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