A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012185



Internal ID18754721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75546018..78211900hg38UCSC Ensembl
Innerchr3:75595169..78261051hg19UCSC Ensembl
Innerchr3:75677859..78343741hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382665883
hg192665883
hg182665883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596185
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ROBO2, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012185
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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