A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515979



Internal ID15096586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125388505..125465747hg38UCSC Ensembl
Innerchr9:128150784..128228026hg19UCSC Ensembl
Innerchr9:127190605..127267847hg18UCSC Ensembl
Innerchr9:125230338..125307580hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3877243
hg1977243
hg1877243
hg1777243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665572, nssv654926, nssv700721
Samples
Known GenesMAPKAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515979
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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