A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049977



Internal ID19139196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55210310..55263496hg38UCSC Ensembl
Innerchr15:55502508..55555694hg19UCSC Ensembl
Innerchr15:53289800..53342986hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3853187
hg1953187
hg1853187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716733
Samples
Known GenesRAB27A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049977
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