A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483001



Internal ID15235475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44208843..44393301hg38UCSC Ensembl
Innerchr10:44704291..44888749hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38184459
hg19184459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996161
Samples
Known GenesCXCL12, LOC100130539
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483001
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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