A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006788



Internal ID19096006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46790474hg38UCSC Ensembl
Innerchr3:46801805..46831964hg19UCSC Ensembl
Innerchr3:46776809..46806968hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3830160
hg1930160
hg1830160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4735n100
Supporting Variantsnssv3590990, nssv3591007, nssv3591017, nssv3590998, nssv3591026, nssv3739721, nssv3591034, nssv3591028, nssv3591004, nssv3591013, nssv3590991, nssv3591033, nssv3591037, nssv3591016, nssv3590997, nssv3591018, nssv3591030, nssv3590988, nssv3591032, nssv3591003, nssv3591001, nssv3591005, nssv3591029, nssv3591012, nssv3590993, nssv3590995, nssv3591021, nssv3591019, nssv3591015, nssv3591008, nssv3591009, nssv3590987, nssv3591027, nssv3591006, nssv3591031, nssv3591014, nssv3590986, nssv3591002, nssv3591035, nssv3591000, nssv3591025, nssv3590989, nssv3591024, nssv3590994, nssv3591020, nssv3591023, nssv3591022, nssv3590996, nssv3591010, nssv3590992, nssv3739720, nssv3591011, nssv3590999, nssv3591036
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006788
Frequency
Sample Size11257
Observed Gain0
Observed Loss54
Observed Complex0
Frequencyn/a


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