A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042945



Internal ID18785476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107707639..107788126hg38UCSC Ensembl
Innerchr13:108359987..108440474hg19UCSC Ensembl
Innerchr13:107157988..107238475hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3880488
hg1980488
hg1880488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525576
Samples
Known GenesFAM155A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042945
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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