A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525929



Internal ID15106536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56350808..56367064hg38UCSC Ensembl
Innerchr16:56384720..56400976hg19UCSC Ensembl
Innerchr16:54942221..54958477hg18UCSC Ensembl
Innerchr16:54942221..54958477hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3816257
hg1916257
hg1816257
hg1716257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702134
Samples
Known GenesAMFR, GNAO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525929
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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