A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515614



Internal ID15096221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:195624547..195671781hg38UCSC Ensembl
Innerchr2:196489271..196536505hg19UCSC Ensembl
Innerchr2:196197516..196244750hg18UCSC Ensembl
Innerchr2:196314777..196362011hg17UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3847235
hg1947235
hg1847235
hg1747235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664107, nssv666345, nssv662080
Samples
Known GenesSLC39A10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515614
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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