A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7139n100



Internal ID20158755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23292116..23464357hg38UCSC Ensembl
chr8:23149629..23321870hg19UCSC Ensembl
chr8:23205574..23377815hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38172242
hg19172242
hg18172242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027563, nsv1029777
Samples
Known GenesENTPD4, LOC100507156, LOXL2, R3HCC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7139n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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