A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515925



Internal ID15096532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86221095..86244605hg38UCSC Ensembl
Innerchr4:87142248..87165758hg19UCSC Ensembl
Innerchr4:87361272..87384782hg18UCSC Ensembl
Innerchr4:87499427..87522937hg17UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3823511
hg1923511
hg1823511
hg1723511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654594, nssv679028, nssv665322, nssv659855
Samples
Known GenesMAPK10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515925
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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