A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042814



Internal ID19132033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107672112..107760954hg38UCSC Ensembl
Innerchr13:108324460..108413302hg19UCSC Ensembl
Innerchr13:107122461..107211303hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3888843
hg1988843
hg1888843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525575
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)nsv1042814
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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