A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516611



Internal ID15097218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:91416806..91476652hg38UCSC Ensembl
InnerchrX:90671805..90731651hg19UCSC Ensembl
InnerchrX:90558461..90618307hg18UCSC Ensembl
InnerchrX:90477950..90537796hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3859847
hg1959847
hg1859847
hg1759847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678922, nssv674070, nssv669524
Samples
Known GenesPABPC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516611
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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