A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009577



Internal ID19098795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75571732hg38UCSC Ensembl
Innerchr3:75427095..75620883hg19UCSC Ensembl
Innerchr3:75509785..75703573hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38193789
hg19193789
hg18193789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3733913, nssv3602330, nssv3602332, nssv3733909, nssv3602335, nssv3602334, nssv3602329, nssv3602328, nssv3733904, nssv3602327, nssv3733899, nssv3733903, nssv3602331, nssv3733905, nssv3733912, nssv3733906, nssv3733910, nssv3602326, nssv3602333, nssv3733908, nssv3733900, nssv3733907, nssv3733911, nssv3733902, nssv3733901
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)nsv1009577
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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