A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013567



Internal ID19102786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9990575..10084686hg38UCSC Ensembl
Innerchr3:10032259..10126370hg19UCSC Ensembl
Innerchr3:10007259..10101370hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3894112
hg1994112
hg1894112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591930
Samples
Known GenesCIDECP, EMC3-AS1, FANCD2, FANCD2OS, LOC401052
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013567
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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