A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051376



Internal ID18793907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30297839..30488448hg38UCSC Ensembl
Innerchr15:30590042..30780651hg19UCSC Ensembl
Innerchr15:28377334..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38190610
hg19190610
hg18190610
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2515n100
Supporting Variantsnssv3546717, nssv3546714, nssv3546715, nssv3546713, nssv3546716
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)nsv1051376
Frequency
Sample Size29084
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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