A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7135n100



Internal ID22793222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21939585..21975988hg38UCSC Ensembl
chr8:21797096..21833499hg19UCSC Ensembl
chr8:21853042..21889445hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3836404
hg1936404
hg1836404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028500, nsv1034335
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7135n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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