A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023052



Internal ID18765585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186323525..186613274hg38UCSC Ensembl
Innerchr4:187244679..187534428hg19UCSC Ensembl
Innerchr4:187481673..187771422hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38289750
hg19289750
hg18289750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5494n100
Supporting Variantsnssv3635632
Samples
Known GenesF11-AS1, FAT1, MTNR1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023052
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