A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519435



Internal ID15446728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45485146..45486810hg38UCSC Ensembl
Innerchr15:45777344..45779008hg19UCSC Ensembl
Innerchr15:43564636..43566300hg18UCSC Ensembl
Innerchr15:43564636..43566300hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381665
hg191665
hg181665
hg171665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696852
Samples
Known GenesSLC30A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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