A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041239



Internal ID18783770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56596747..56666830hg38UCSC Ensembl
Innerchr15:56888945..56959028hg19UCSC Ensembl
Innerchr15:54676237..54746320hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3870084
hg1970084
hg1870084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553585
Samples
Known GenesZNF280D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041239
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