A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053553



Internal ID19142772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81703904..81795068hg38UCSC Ensembl
Innerchr15:81996245..82087409hg19UCSC Ensembl
Innerchr15:79783300..79874464hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3891165
hg1991165
hg1891165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n100
Supporting Variantsnssv3554601, nssv3554602
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053553
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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