A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998066



Internal ID19157603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75459391hg38UCSC Ensembl
Innerchr3:75427095..75508542hg19UCSC Ensembl
Innerchr3:75509785..75591232hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3881448
hg1981448
hg1881448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4775n100
Supporting Variantsnssv3602011, nssv3733032
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)nsv998066
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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