A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528587



Internal ID15455880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:2143649..2200407hg38UCSC Ensembl
Innerchr2:2147421..2204179hg19UCSC Ensembl
Innerchr2:2126428..2183186hg18UCSC Ensembl
Innerchr2:2117718..2174476hg17UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3856759
hg1956759
hg1856759
hg1756759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705212
Samples
Known GenesMYT1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528587
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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