A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005724



Internal ID19094941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75347667..75832110hg38UCSC Ensembl
Innerchr3:75396818..75881261hg19UCSC Ensembl
Innerchr3:75479508..75963951hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38484444
hg19484444
hg18484444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4773n100
Supporting Variantsnssv3732980
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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