A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014265



Internal ID19103486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68818494..68872597hg38UCSC Ensembl
Innerchr3:68867645..68921748hg19UCSC Ensembl
Innerchr3:68950335..69004438hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3854104
hg1954104
hg1854104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594150
Samples
Known GenesFAM19A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014265
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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