A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519480



Internal ID15446773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87550822..87619348hg38UCSC Ensembl
Innerchr13:88203077..88271603hg19UCSC Ensembl
Innerchr13:87001078..87069604hg18UCSC Ensembl
Innerchr13:87001078..87069604hg17UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3868527
hg1968527
hg1868527
hg1768527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696875
Samples
Known GenesMIR4500, MIR4500HG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519480
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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