A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv67n21



Internal ID20131788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44250972..44277071hg38UCSC Ensembl
chr11:44272522..44298621hg19UCSC Ensembl
chr11:44229098..44255197hg18UCSC Ensembl
chr11:44229098..44255197hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3826100
hg1926100
hg1826100
hg1726100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526910, nsv517357
Samples
Known GenesALX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv67n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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