A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006919



Internal ID19096137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75400451..75458729hg38UCSC Ensembl
Innerchr3:75449602..75507880hg19UCSC Ensembl
Innerchr3:75532292..75590570hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3858279
hg1958279
hg1858279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4781n100
Supporting Variantsnssv3733700, nssv3733699
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)nsv1006919
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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