A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037667



Internal ID19126886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97257376..97302714hg38UCSC Ensembl
Innerchr15:97800606..97845944hg19UCSC Ensembl
Innerchr15:95601610..95646948hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3845339
hg1945339
hg1845339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555286, nssv3555285
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)nsv1037667
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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