A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552384



Internal ID18850665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49549247..49598592hg38UCSC Ensembl
Innerchr15:49841444..49890789hg19UCSC Ensembl
Innerchr15:47628736..47678081hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3849346
hg1949346
hg1849346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040578
Supporting Variants
Samples
Known GenesFAM227B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552384
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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