A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009813



Internal ID19099032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75636809hg38UCSC Ensembl
Innerchr3:75427095..75685960hg19UCSC Ensembl
Innerchr3:75509785..75768650hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38258866
hg19258866
hg18258866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3596086, nssv3596089, nssv3596087, nssv3596090, nssv3596088
Samples
Known GenesFAM86DP, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009813
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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