A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048311



Internal ID19137530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27672432..27689357hg38UCSC Ensembl
Innerchr15:27917578..27934503hg19UCSC Ensembl
Innerchr15:25591173..25608098hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3816926
hg1916926
hg1816926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2488n100
Supporting Variantsnssv3545654
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)nsv1048311
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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