A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666537



Internal ID15403189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151278051..151294661hg38UCSC Ensembl
InnerchrX:150446523..150463133hg19UCSC Ensembl
InnerchrX:150197181..150213791hg18UCSC Ensembl
InnerchrX:150117091..150133701hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3816611
hg1916611
hg1816611
hg1716611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517397
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666537
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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