A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516158



Internal ID15096765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:154790808..154831402hg38UCSC Ensembl
InnerchrX:154019083..154059677hg19UCSC Ensembl
InnerchrX:153672277..153712871hg18UCSC Ensembl
InnerchrX:153582787..153623381hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3840595
hg1940595
hg1840595
hg1740595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693656, nssv681519, nssv674697, nssv677047, nssv666538, nssv689388, nssv671099, nssv684383, nssv680729, nssv694576, nssv673197, nssv662790, nssv671736
Samples
Known GenesMPP1, SMIM9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516158
Frequency
Sample Size2026
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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