A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528991



Internal ID15109598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:91725977..91732605hg38UCSC Ensembl
Innerchr1:92191534..92198162hg19UCSC Ensembl
Innerchr1:91964122..91970750hg18UCSC Ensembl
Innerchr1:91903555..91910183hg17UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386629
hg196629
hg186629
hg176629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705693
Samples
Known GenesTGFBR3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528991
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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