A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046270



Internal ID19135489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89144402..89193689hg38UCSC Ensembl
Innerchr13:89796656..89845943hg19UCSC Ensembl
Innerchr13:88594657..88643944hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3849288
hg1949288
hg1849288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1726n100
Supporting Variantsnssv3525457
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046270
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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