A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038407



Internal ID19127626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94201707..94243100hg38UCSC Ensembl
Innerchr14:94668044..94709437hg19UCSC Ensembl
Innerchr14:93737797..93779190hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3841394
hg1941394
hg1841394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532608
Samples
Known GenesPPP4R4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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