A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv729849



Internal ID15677119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:186672066..186674232hg38UCSC Ensembl
Innerchr1:186641198..186643364hg19UCSC Ensembl
Innerchr1:184907821..184909987hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg382167
hg192167
hg182167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548402
Supporting Variants
Samples
Known GenesPTGS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv729849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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