A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527046



Internal ID15107653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15760765..15784320hg38UCSC Ensembl
Innerchr1:16087260..16110815hg19UCSC Ensembl
Innerchr1:15959847..15983402hg18UCSC Ensembl
Innerchr1:15832566..15856121hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3823556
hg1923556
hg1823556
hg1723556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703422
Samples
Known GenesFBLIM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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