A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528005



Internal ID15108612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15247097..15264373hg38UCSC Ensembl
InnerchrX:15265219..15282495hg19UCSC Ensembl
InnerchrX:15175140..15192416hg18UCSC Ensembl
InnerchrX:15024876..15042152hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3817277
hg1917277
hg1817277
hg1717277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704531
Samples
Known GenesASB9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528005
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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