A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037929



Internal ID19127148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24009673..24053238hg38UCSC Ensembl
Innerchr14:24478882..24522447hg19UCSC Ensembl
Innerchr14:23548722..23592287hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3843566
hg1943566
hg1843566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1848n100
Supporting Variantsnssv3528451
Samples
Known GenesDHRS4L1, LRRC16B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037929
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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