A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7165n100



Internal ID20158781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38200929..38249049hg38UCSC Ensembl
chr8:38058447..38106567hg19UCSC Ensembl
chr8:38177604..38225724hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3848121
hg1948121
hg1848121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026694, nsv1031384, nsv1030909
Samples
Known GenesBAG4, DDHD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7165n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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