A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5776n54



Internal ID20139200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75724647..75733488hg38UCSC Ensembl
chr17:73720727..73729569hg19UCSC Ensembl
chr17:71232322..71241164hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg388842
hg198843
hg188843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576036, nsv576037
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5776n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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