A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593972



Internal ID18892253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68304041..68339675hg38UCSC Ensembl
Innerchr3:68353191..68388825hg19UCSC Ensembl
Innerchr3:68435881..68471515hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3835635
hg1935635
hg1835635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010992
Supporting Variants
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)nssv3593972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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