A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516579



Internal ID15097186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13796604..13796659hg38UCSC Ensembl
Innerchr10:13838604..13838659hg19UCSC Ensembl
Innerchr10:13878610..13878665hg18UCSC Ensembl
Innerchr10:13878610..13878665hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
hg1756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669295, nssv680572, nssv682445, nssv686154, nssv689911
Samples
Known GenesFRMD4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516579
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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