A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998752



Internal ID19158288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75537642hg38UCSC Ensembl
Innerchr3:75415863..75586793hg19UCSC Ensembl
Innerchr3:75498553..75669483hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38170931
hg19170931
hg18170931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3594925, nssv3594935, nssv3594931, nssv3594927, nssv3594928, nssv3594924, nssv3594929, nssv3594926, nssv3732987, nssv3594184, nssv3594933, nssv3594183, nssv3594923, nssv3594934, nssv3594930, nssv3594932
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)nsv998752
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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