A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067082



Internal ID19156301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51639087..51655602hg38UCSC Ensembl
Innerchr19:52142340..52158855hg19UCSC Ensembl
Innerchr19:56834152..56850667hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3816516
hg1916516
hg1816516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3624n100
Supporting Variantsnssv3575006
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)nsv1067082
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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