A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014754



Internal ID19103971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75489766hg38UCSC Ensembl
Innerchr3:75421158..75538917hg19UCSC Ensembl
Innerchr3:75503848..75621607hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38117760
hg19117760
hg18117760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3732988, nssv3594966
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014754
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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