A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153494



Internal ID15877751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97676842..97894707hg38UCSC Ensembl
Innerchr4:98597993..98815858hg19UCSC Ensembl
Innerchr4:98817016..99034881hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38217866
hg19217866
hg18217866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594936
Supporting Variants
SamplesHGDP01040
Known GenesSTPG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153494
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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