A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049743



Internal ID19138962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70146633..70170613hg38UCSC Ensembl
Innerchr15:70438972..70462952hg19UCSC Ensembl
Innerchr15:68226026..68250006hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3823981
hg1923981
hg1823981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553667, nssv3553666, nssv3553668
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)nsv1049743
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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