A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517497



Internal ID15444790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56925030..56925686hg38UCSC Ensembl
InnerchrX:56951463..56952119hg19UCSC Ensembl
InnerchrX:56968188..56968844hg18UCSC Ensembl
InnerchrX:56834484..56835140hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg38657
hg19657
hg18657
hg17657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669767, nssv652190, nssv662038, nssv655599
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517497
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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