A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708841



Internal ID15656111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3271745..3286557hg38UCSC Ensembl
Innerchr1:3188309..3203121hg19UCSC Ensembl
Innerchr1:3178169..3192981hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3814813
hg1914813
hg1814813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545121
Supporting Variants
Samples
Known GenesPRDM16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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