A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3113n100



Internal ID22789200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18410504..18629085hg38UCSC Ensembl
chr17:18313818..18532398hg19UCSC Ensembl
chr17:18254543..18473123hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38218582
hg19218581
hg18218581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058346, nsv1056622, nsv1060524
Samples
Known GenesCCDC144B, FAM106A, FLJ35934, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3113n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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