A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv527n21



Internal ID22766719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118388145..118846744hg38UCSC Ensembl
chrX:117522108..117980707hg19UCSC Ensembl
chrX:117406136..117864735hg18UCSC Ensembl
chrX:117303990..117762589hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38458600
hg19458600
hg18458600
hg17458600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517257, nsv524583
Samples
Known GenesDOCK11, IL13RA1, WDR44, ZCCHC12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv527n21
Frequency
Sample Size2026
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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