A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078878



Internal ID15932064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7277959..7458045hg38UCSC Ensembl
Innerchr7:7317590..7497676hg19UCSC Ensembl
Innerchr7:7284115..7464201hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38180087
hg19180087
hg18180087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606039
Supporting Variants
Samples
Known GenesCOL28A1, LOC101927354
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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