A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525946



Internal ID15453239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:86595708..86706107hg38UCSC Ensembl
InnerchrX:85850711..85961110hg19UCSC Ensembl
InnerchrX:85737367..85847766hg18UCSC Ensembl
InnerchrX:85656856..85767255hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38110400
hg19110400
hg18110400
hg17110400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702152
Samples
Known GenesDACH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525946
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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