A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523008



Internal ID15450301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:46151138..46218512hg38UCSC Ensembl
InnerchrX:46010573..46077947hg19UCSC Ensembl
InnerchrX:45895517..45962891hg18UCSC Ensembl
InnerchrX:45766827..45834201hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3867375
hg1967375
hg1867375
hg1767375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698680
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523008
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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