A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524807



Internal ID15105414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19674533..19764302hg38UCSC Ensembl
Innerchr7:19714156..19803925hg19UCSC Ensembl
Innerchr7:19680681..19770450hg18UCSC Ensembl
Innerchr7:19487396..19577165hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3889770
hg1989770
hg1889770
hg1789770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700799
Samples
Known GenesMIR3146, TMEM196, TWISTNB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524807
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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