A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035987



Internal ID19125206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84921267..84950132hg38UCSC Ensembl
Innerchr15:85464498..85493363hg19UCSC Ensembl
Innerchr15:83265502..83294367hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3828866
hg1928866
hg1828866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2646n100
Supporting Variantsnssv3555060
Samples
Known GenesSLC28A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035987
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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