A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999551



Internal ID19159088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86054929..86070837hg38UCSC Ensembl
Innerchr4:86976082..86991990hg19UCSC Ensembl
Innerchr4:87195106..87211014hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3815909
hg1915909
hg1815909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5333n100
Supporting Variantsnssv3633910, nssv3633916, nssv3633911, nssv3742876, nssv3633912, nssv3633915, nssv3633914, nssv3633913
Samples
Known GenesMAPK10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999551
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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