A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051563



Internal ID19140782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19014957..19954095hg38UCSC Ensembl
Innerchr14:19602662..20422254hg19UCSC Ensembl
Innerchr14:18672662..19492094hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38939139
hg19819593
hg18819433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1766n100
Supporting Variantsnssv3529623, nssv3529624
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)nsv1051563
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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