A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049801



Internal ID19139020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74104187..74131264hg38UCSC Ensembl
Innerchr14:74570890..74597967hg19UCSC Ensembl
Innerchr14:73640643..73667720hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827078
hg1927078
hg1827078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1939n100
Supporting Variantsnssv3531175, nssv3531178, nssv3531180, nssv3713526, nssv3531173, nssv3531174, nssv3531179, nssv3531181, nssv3531172, nssv3531177, nssv3531176
Samples
Known GenesLIN52
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049801
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer