A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004679



Internal ID19093896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:75072101..75170360hg38UCSC Ensembl
Innerchr4:75997311..76095570hg19UCSC Ensembl
Innerchr4:76216335..76314594hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3898260
hg1998260
hg1898260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742870
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004679
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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