A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036897



Internal ID19126116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92668761..92696158hg38UCSC Ensembl
Innerchr15:93211991..93239388hg19UCSC Ensembl
Innerchr15:91012995..91040392hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3827398
hg1927398
hg1827398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555230
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)nsv1036897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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