A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594150



Internal ID18892431
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 StatusS
Merged Variantsnsv1014265
Supporting Variants
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)nssv3594150
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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