A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3717947



Internal ID19016228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60025802..60062320hg38UCSC Ensembl
Innerchr15:60318001..60354519hg19UCSC Ensembl
Innerchr15:58105293..58141811hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3836519
hg1936519
hg1836519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044105
Supporting Variants
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)nssv3717947
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