A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012818



Internal ID19102035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75590743hg38UCSC Ensembl
Innerchr3:75415863..75639894hg19UCSC Ensembl
Innerchr3:75498553..75722584hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38224032
hg19224032
hg18224032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3594952, nssv3594940, nssv3594939, nssv3594946, nssv3594950, nssv3594945, nssv3594941, nssv3594953, nssv3594944, nssv3594951, nssv3594943, nssv3594948, nssv3594949, nssv3594942, nssv3594947
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)nsv1012818
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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