A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012911



Internal ID19102128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75625450hg38UCSC Ensembl
Innerchr3:75421158..75674601hg19UCSC Ensembl
Innerchr3:75503848..75757291hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38253444
hg19253444
hg18253444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3733026
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)nsv1012911
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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