A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066339



Internal ID19155558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39866378..39921996hg38UCSC Ensembl
Innerchr19:40357018..40427903hg19UCSC Ensembl
Innerchr19:45048858..45119743hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3855619
hg1970886
hg1870886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568209
Samples
Known GenesFCGBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066339
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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