A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054615



Internal ID19143834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47762752..47808236hg38UCSC Ensembl
Innerchr14:48231955..48277439hg19UCSC Ensembl
Innerchr14:47301705..47347189hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3845485
hg1945485
hg1845485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n100
Supporting Variantsnssv3530955, nssv3713484, nssv3713478, nssv3713483, nssv3530974, nssv3530973, nssv3530971, nssv3530956, nssv3713479, nssv3713480, nssv3530970, nssv3530966, nssv3530972, nssv3530958, nssv3531691, nssv3530975, nssv3530963, nssv3530968, nssv3530959, nssv3530967, nssv3530961, nssv3530964, nssv3530976, nssv3713481, nssv3530960, nssv3713482, nssv3530969, nssv3530954, nssv3530977, nssv3530957, nssv3530965, nssv3530962
Samples
Known GenesLINC00648
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054615
Frequency
Sample Size11257
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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