A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066451



Internal ID18808982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35375887hg38UCSC Ensembl
Innerchr19:35849481..35866789hg19UCSC Ensembl
Innerchr19:40541321..40558629hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3817309
hg1917309
hg1817309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3521n100
Supporting Variantsnssv3724512, nssv3568138
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066451
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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