A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525751



Internal ID15106358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38163004..38169273hg38UCSC Ensembl
InnerchrX:38022257..38028526hg19UCSC Ensembl
InnerchrX:37907201..37913470hg18UCSC Ensembl
InnerchrX:37778474..37784743hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg386270
hg196270
hg186270
hg176270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701918
Samples
Known GenesSRPX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525751
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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