A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053853



Internal ID18796384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30338750..30468834hg38UCSC Ensembl
Innerchr15:30630953..30761037hg19UCSC Ensembl
Innerchr15:28418245..28548329hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38130085
hg19130085
hg18130085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2521n100
Supporting Variantsnssv3546774
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053853
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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