A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525695



Internal ID15106302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75136060..75153826hg38UCSC Ensembl
Innerchr2:75363186..75380952hg19UCSC Ensembl
Innerchr2:75216694..75234460hg18UCSC Ensembl
Innerchr2:75274841..75292607hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3817767
hg1917767
hg1817767
hg1717767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701854
Samples
Known GenesTACR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525695
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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