A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036638



Internal ID18779169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15912446..16358900hg38UCSC Ensembl
Innerchr12:16065380..16511834hg19UCSC Ensembl
Innerchr12:15956647..16403101hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38446455
hg19446455
hg18446455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505334
Samples
Known GenesDERA, MGST1, SLC15A5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036638
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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