A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997646



Internal ID19157183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75527398hg38UCSC Ensembl
Innerchr3:75427095..75576549hg19UCSC Ensembl
Innerchr3:75509785..75659239hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38149455
hg19149455
hg18149455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3602228, nssv3602230, nssv3733882, nssv3602229, nssv3733883
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)nsv997646
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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