A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049204



Internal ID19138423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44712945..44764023hg38UCSC Ensembl
Innerchr14:45182148..45233226hg19UCSC Ensembl
Innerchr14:44251898..44302976hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3851079
hg1951079
hg1851079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1903n100
Supporting Variantsnssv3530433
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049204
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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