A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044674



Internal ID19133893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74104530..74132353hg38UCSC Ensembl
Innerchr14:74571233..74599056hg19UCSC Ensembl
Innerchr14:73640986..73668809hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827824
hg1927824
hg1827824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1939n100
Supporting Variantsnssv3531197
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)nsv1044674
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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