A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011217



Internal ID19100434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97333585..97420162hg38UCSC Ensembl
Innerchr4:98254736..98341313hg19UCSC Ensembl
Innerchr4:98473759..98560336hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3886578
hg1986578
hg1886578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3630992
Samples
Known GenesSTPG2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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