A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045781



Internal ID19135000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85427976..85451841hg38UCSC Ensembl
Innerchr13:86002111..86025976hg19UCSC Ensembl
Innerchr13:84900112..84923977hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3823866
hg1923866
hg1823866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525418
Samples
Known GenesLINC00351
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045781
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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