A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078881



Internal ID15932067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7433932..7531789hg38UCSC Ensembl
Innerchr7:7473563..7571420hg19UCSC Ensembl
Innerchr7:7440088..7537945hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3897858
hg1997858
hg1897858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606043
Supporting Variants
Samples
Known GenesCOL28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer