A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056941



Internal ID18799472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35375830hg38UCSC Ensembl
Innerchr19:35849481..35866732hg19UCSC Ensembl
Innerchr19:40541321..40558572hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3817252
hg1917252
hg1817252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3521n100
Supporting Variantsnssv3568136
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)nsv1056941
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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