A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065199



Internal ID19154418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51639087..51662186hg38UCSC Ensembl
Innerchr19:52142340..52165439hg19UCSC Ensembl
Innerchr19:56834152..56857251hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3823100
hg1923100
hg1823100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3624n100
Supporting Variantsnssv3575007
Samples
Known GenesSIGLEC14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065199
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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