A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2651n100



Internal ID22788738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85789733..85807041hg38UCSC Ensembl
chr15:86332964..86350272hg19UCSC Ensembl
chr15:84133968..84151276hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3817309
hg1917309
hg1817309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044574, nsv1042023
Samples
Known GenesKLHL25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2651n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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