A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040193



Internal ID19129412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93598378..93621076hg38UCSC Ensembl
Innerchr15:94141607..94164305hg19UCSC Ensembl
Innerchr15:91942611..91965309hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3822699
hg1922699
hg1822699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2663n100
Supporting Variantsnssv3555250, nssv3555254, nssv3555251, nssv3555253, nssv3555249, nssv3555246, nssv3718201, nssv3555247, nssv3718202, nssv3718203, nssv3718200, nssv3555248, nssv3555252, nssv3555244, nssv3555245
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)nsv1040193
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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