A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002149



Internal ID19091366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75493683hg38UCSC Ensembl
Innerchr3:75427095..75542834hg19UCSC Ensembl
Innerchr3:75509785..75625524hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38115740
hg19115740
hg18115740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3602046, nssv3733067, nssv3733066, nssv3733059, nssv3733061, nssv3733063, nssv3602049, nssv3602045, nssv3733058, nssv3602055, nssv3602042, nssv3602044, nssv3602048, nssv3602053, nssv3602057, nssv3602052, nssv3602056, nssv3602054, nssv3602047, nssv3602050, nssv3602051, nssv3733068, nssv3602058, nssv3733065, nssv3733064, nssv3602043, nssv3733062, nssv3733060
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)nsv1002149
Frequency
Sample Size11257
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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