A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039817



Internal ID19129036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89773711..90232017hg38UCSC Ensembl
Innerchr13:90425965..90884271hg19UCSC Ensembl
Innerchr13:89223966..89682272hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38458307
hg19458307
hg18458307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525470
Samples
Known GenesLINC00559, MIR622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039817
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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