A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552444



Internal ID18850725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54845408..55260357hg38UCSC Ensembl
Innerchr15:55137606..55552555hg19UCSC Ensembl
Innerchr15:52924898..53339847hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38414950
hg19414950
hg18414950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039471
Supporting Variants
Samples
Known GenesRAB27A, RSL24D1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552444
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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