A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522795



Internal ID15103402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201419020..201420171hg38UCSC Ensembl
Innerchr1:201388148..201389299hg19UCSC Ensembl
Innerchr1:199654771..199655922hg18UCSC Ensembl
Innerchr1:198119805..198120956hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381152
hg191152
hg181152
hg171152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698439
Samples
Known GenesTNNI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522795
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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