A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051558



Internal ID19140777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78023200..78072605hg38UCSC Ensembl
Innerchr15:78315542..78364947hg19UCSC Ensembl
Innerchr15:76102597..76152002hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3849406
hg1949406
hg1849406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718095
Samples
Known GenesTBC1D2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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