A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3606102



Internal ID18557697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141516537..141563773hg38UCSC Ensembl
Innerchr3:141235379..141282615hg19UCSC Ensembl
Innerchr3:142718069..142765305hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3847237
hg1947237
hg1847237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014365
Supporting Variants
Samples
Known GenesRASA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3606102
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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