A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037842



Internal ID19127061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94178251..94249384hg38UCSC Ensembl
Innerchr14:94644588..94715721hg19UCSC Ensembl
Innerchr14:93714341..93785474hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3871134
hg1971134
hg1871134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1959n100
Supporting Variantsnssv3532602
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)nsv1037842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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