A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657149



Internal ID18955430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79175971..79223365hg38UCSC Ensembl
Innerchr7:78805287..78852681hg19UCSC Ensembl
Innerchr7:78643223..78690617hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3847395
hg1947395
hg1847395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032979
Supporting Variants
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)nssv3657149
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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