A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040620



Internal ID19129839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26050543..26087960hg38UCSC Ensembl
Innerchr15:26295690..26333107hg19UCSC Ensembl
Innerchr15:23846783..23884200hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3837418
hg1937418
hg1837418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545631
Samples
Known GenesLOC100128714
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040620
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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