A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054846



Internal ID19144065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107516630..107673495hg38UCSC Ensembl
Innerchr13:108168978..108325843hg19UCSC Ensembl
Innerchr13:106966979..107123844hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38156866
hg19156866
hg18156866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713302
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)nsv1054846
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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