A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566671



Internal ID18518266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35370865hg38UCSC Ensembl
Innerchr19:35849481..35861767hg19UCSC Ensembl
Innerchr19:40541321..40553607hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812287
hg1912287
hg1812287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060131
Supporting Variants
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)nssv3566671
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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