A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519108



Internal ID15099715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70257625..70259092hg38UCSC Ensembl
InnerchrX:69477475..69478942hg19UCSC Ensembl
InnerchrX:69394200..69395667hg18UCSC Ensembl
InnerchrX:69260496..69261963hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg381468
hg191468
hg181468
hg171468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696584
Samples
Known GenesP2RY4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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