A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517375



Internal ID15444668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54569818..54614994hg38UCSC Ensembl
InnerchrX:54596251..54641427hg19UCSC Ensembl
InnerchrX:54612976..54658152hg18UCSC Ensembl
InnerchrX:54479272..54524448hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3845177
hg1945177
hg1845177
hg1745177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673861, nssv694173, nssv657826, nssv685680, nssv672608, nssv670088, nssv673549, nssv680730, nssv675661, nssv682193, nssv651841, nssv694499, nssv668748, nssv670429, nssv674764, nssv664444
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517375
Frequency
Sample Size2026
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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