A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523441



Internal ID18475036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48337128..48351221hg38UCSC Ensembl
Innerchr13:48911264..48925357hg19UCSC Ensembl
Innerchr13:47809265..47823358hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3814094
hg1914094
hg1814094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042504
Supporting Variants
Samples
Known GenesRB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523441
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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