A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153180



Internal ID15873808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152647942..152677136hg38UCSC Ensembl
Innerchr4:153569094..153598288hg19UCSC Ensembl
Innerchr4:153788544..153817738hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3829195
hg1929195
hg1829195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595743
Supporting Variants
SamplesHGDP00364
Known GenesTMEM154
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153180
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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