A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037442



Internal ID18779973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66423144..66485732hg38UCSC Ensembl
Innerchr15:66715482..66778070hg19UCSC Ensembl
Innerchr15:64502536..64565124hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3862589
hg1962589
hg1862589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553648
Samples
Known GenesMAP2K1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037442
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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