A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051850



Internal ID18794381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43222549..44531691hg38UCSC Ensembl
Innerchr14:43691752..45000894hg19UCSC Ensembl
Innerchr14:42761502..44070644hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381309143
hg191309143
hg181309143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530222
Samples
Known GenesFSCB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051850
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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