A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041793



Internal ID19131012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32217691..32387416hg38UCSC Ensembl
Innerchr15:32509892..32679617hg19UCSC Ensembl
Innerchr15:30297184..30466909hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38169726
hg19169726
hg18169726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2541n100
Supporting Variantsnssv3547802, nssv3547801, nssv3547804, nssv3547803
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)nsv1041793
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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