A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003779



Internal ID19092997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68421749..68467974hg38UCSC Ensembl
Innerchr3:68470899..68517125hg19UCSC Ensembl
Innerchr3:68553589..68599815hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3846226
hg1946227
hg1846227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732975
Samples
Known GenesFAM19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003779
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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