A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048195



Internal ID19137414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74104187..74145313hg38UCSC Ensembl
Innerchr14:74570890..74612016hg19UCSC Ensembl
Innerchr14:73640643..73681769hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3841127
hg1941127
hg1841127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1940n100
Supporting Variantsnssv3531186
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)nsv1048195
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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