A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035364



Internal ID18777895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:104554529..104609927hg38UCSC Ensembl
Innerchr12:104948307..105003705hg19UCSC Ensembl
Innerchr12:103472437..103527835hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3855399
hg1955399
hg1855399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524870
Samples
Known GenesCHST11, MIR3922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035364
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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