A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039191



Internal ID19128410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19955201hg38UCSC Ensembl
Innerchr14:19795573..20423360hg19UCSC Ensembl
Innerchr14:18865573..19493200hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38724253
hg19627788
hg18627628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1768n100
Supporting Variantsnssv3711120, nssv3527269, nssv3527270, nssv3527271
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039191
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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