A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1081661



Internal ID15588161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28534721..28535491hg38UCSC Ensembl
Innerchr7:28574339..28575109hg19UCSC Ensembl
Innerchr7:28540864..28541634hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38771
hg19771
hg18771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606477
Supporting Variants
Samples
Known GenesCREB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1081661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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