A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010768



Internal ID18753300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9502870..9873902hg38UCSC Ensembl
Innerchr3:9544554..9915586hg19UCSC Ensembl
Innerchr3:9519554..9890586hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38371033
hg19371033
hg18371033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591929
Samples
Known GenesARPC4, ARPC4-TTLL3, BRPF1, CAMK1, CIDEC, CPNE9, LHFPL4, MTMR14, OGG1, RPUSD3, TADA3, TTLL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010768
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer