A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004017



Internal ID19093234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75511978hg38UCSC Ensembl
Innerchr3:75415863..75561129hg19UCSC Ensembl
Innerchr3:75498553..75643819hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38145267
hg19145267
hg18145267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3594182, nssv3732986, nssv3594181
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)nsv1004017
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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