A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044444



Internal ID18786975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:48331224..48343787hg38UCSC Ensembl
Innerchr12:48725007..48737570hg19UCSC Ensembl
Innerchr12:47011274..47023837hg18UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3812564
hg1912564
hg1812564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523520
Samples
Known GenesZNF641
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044444
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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