A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708768



Internal ID15656038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3167468..3168255hg38UCSC Ensembl
Innerchr1:3084032..3084819hg19UCSC Ensembl
Innerchr1:3073892..3074679hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545102
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)nssv708768
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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