A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037745



Internal ID18780276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064523..31100684hg38UCSC Ensembl
Innerchr15:31356726..31392887hg19UCSC Ensembl
Innerchr15:29144018..29180179hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3836162
hg1936162
hg1836162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2534n100
Supporting Variantsnssv3721588
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037745
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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