A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525455



Internal ID15106062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:1956204..2025860hg38UCSC Ensembl
Innerchr12:2065370..2135026hg19UCSC Ensembl
Innerchr12:1935631..2005287hg18UCSC Ensembl
Innerchr12:1935631..2005287hg17UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3869657
hg1969657
hg1869657
hg1769657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701583
Samples
Known GenesDCP1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525455
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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