A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528082



Internal ID15455375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95241967..95246573hg38UCSC Ensembl
Innerchr15:95785196..95789802hg19UCSC Ensembl
Innerchr15:93586200..93590806hg18UCSC Ensembl
Innerchr15:93586200..93590806hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg384607
hg194607
hg184607
hg174607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704618
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528082
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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