A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066553



Internal ID18809084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35207735..35258660hg38UCSC Ensembl
Innerchr19:35698638..35749563hg19UCSC Ensembl
Innerchr19:40390478..40441403hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3850926
hg1950926
hg1850926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566599
Samples
Known GenesFAM187B, LSR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066553
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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