A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522101



Internal ID15449394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:175140381..175182047hg38UCSC Ensembl
Innerchr1:175109517..175151183hg19UCSC Ensembl
Innerchr1:173376140..173417806hg18UCSC Ensembl
Innerchr1:171841174..171882840hg17UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3841667
hg1941667
hg1841667
hg1741667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694873
Samples
Known GenesKIAA0040, TNN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522101
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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