A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041150



Internal ID18783681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30230905..30488448hg38UCSC Ensembl
Innerchr15:30523108..30780651hg19UCSC Ensembl
Innerchr15:28310400..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38257544
hg19257544
hg18257544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2509n100
Supporting Variantsnssv3546668, nssv3721548
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)nsv1041150
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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