A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555331



Internal ID18853612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101123620..101153676hg38UCSC Ensembl
Innerchr15:101663825..101693881hg19UCSC Ensembl
Innerchr15:99481348..99511404hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3830057
hg1930057
hg1830057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036288
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)nssv3555331
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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