A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516515



Internal ID15443808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144626197..144740259hg38UCSC Ensembl
InnerchrX:143707718..143821780hg19UCSC Ensembl
InnerchrX:143515360..143629479hg18UCSC Ensembl
InnerchrX:143413214..143527333hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38114063
hg19114063
hg18114120
hg17114120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673938, nssv688899, nssv680331, nssv685703, nssv698986, nssv682507, nssv685410, nssv668782, nssv672024, nssv691148, nssv672973, nssv688301, nssv695473
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516515
Frequency
Sample Size2026
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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