A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570561



Internal ID16357970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94417126..94457977hg38UCSC Ensembl
Innerchr15:94960355..95001206hg19UCSC Ensembl
Innerchr15:92761359..92802210hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3840852
hg1940852
hg1840852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv849044
Samples
Known GenesMCTP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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