A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654926



Internal ID15044892
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515979
Supporting Variants
Samples
Known GenesMAPKAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654926
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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