A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844323



Internal ID15791593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67570774..67585107hg38UCSC Ensembl
Innerchr15:67863112..67877445hg19UCSC Ensembl
Innerchr15:65650166..65664499hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3814334
hg1914334
hg1814334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569800
Supporting Variants
Samples
Known GenesMAP2K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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