A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048854



Internal ID19138073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37036233..37077154hg38UCSC Ensembl
Innerchr14:37505438..37546359hg19UCSC Ensembl
Innerchr14:36575189..36616110hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3840922
hg1940922
hg1840922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1870n100
Supporting Variantsnssv3528626
Samples
Known GenesSLC25A21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048854
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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