A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040213



Internal ID19129432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30297839..30376369hg38UCSC Ensembl
Innerchr15:30590042..30668572hg19UCSC Ensembl
Innerchr15:28377334..28455864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3878531
hg1978531
hg1878531
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3546706, nssv3546705
Samples
Known GenesCHRFAM7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040213
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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