A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555239



Internal ID18853520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93598378..93619013hg38UCSC Ensembl
Innerchr15:94141607..94162242hg19UCSC Ensembl
Innerchr15:91942611..91963246hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3820636
hg1920636
hg1820636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043930
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)nssv3555239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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