A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041464



Internal ID19130683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93598378..93620120hg38UCSC Ensembl
Innerchr15:94141607..94163349hg19UCSC Ensembl
Innerchr15:91942611..91964353hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821743
hg1921743
hg1821743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2663n100
Supporting Variantsnssv3555240
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)nsv1041464
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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