A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703524



Internal ID15440176
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527137
Supporting Variants
Samples
Known GenesMYT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703524
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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