A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052639



Internal ID19141858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62295263..62318032hg38UCSC Ensembl
Innerchr15:62587462..62610231hg19UCSC Ensembl
Innerchr15:60374754..60397523hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3822770
hg1922770
hg1822770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717949, nssv3553642, nssv3553641, nssv3553640
Samples
Known GenesMIR8067
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052639
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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