A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708800



Internal ID15656070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3167572..3169932hg38UCSC Ensembl
Innerchr1:3084136..3086496hg19UCSC Ensembl
Innerchr1:3073996..3076356hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382361
hg192361
hg182361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545112
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)nssv708800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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