A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527137



Internal ID15454430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64205167..64215178hg38UCSC Ensembl
Innerchr20:62836520..62846531hg19UCSC Ensembl
Innerchr20:62306964..62316975hg18UCSC Ensembl
Innerchr20:62306964..62316975hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810012
hg1910012
hg1810012
hg1710012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703524
Samples
Known GenesMYT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527137
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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