A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv513n21



Internal ID22766705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44533159..44740455hg38UCSC Ensembl
chrX:44392405..44599701hg19UCSC Ensembl
chrX:44277349..44484645hg18UCSC Ensembl
chrX:44148659..44355955hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38207297
hg19207297
hg18207297
hg17207297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527721, nsv527378
Samples
Known GenesFUNDC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv513n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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