A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528203



Internal ID15455496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8107901..8206085hg38UCSC Ensembl
InnerchrX:8075942..8174126hg19UCSC Ensembl
InnerchrX:8035942..8134126hg18UCSC Ensembl
InnerchrX:7885678..7983862hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3898185
hg1998185
hg1898185
hg1798185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704764
Samples
Known GenesMIR651, VCX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528203
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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