A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039354



Internal ID19128573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107244161..107265107hg38UCSC Ensembl
Innerchr13:107896509..107917455hg19UCSC Ensembl
Innerchr13:106694510..106715456hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3820947
hg1920947
hg1820947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525570
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)nsv1039354
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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