A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034972



Internal ID18777503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105294788..105357360hg38UCSC Ensembl
Innerchr8:106307016..106369588hg19UCSC Ensembl
Innerchr8:106376192..106438764hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3862573
hg1962573
hg1862573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691263
Samples
Known GenesZFPM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034972
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