A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5787n54



Internal ID18997963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77270084..77281555hg38UCSC Ensembl
chr17:75266166..75277637hg19UCSC Ensembl
chr17:72777761..72789232hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3811472
hg1911472
hg1811472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576080, nsv576090, nsv576086, nsv576088, nsv576089
Samples
Known GenesSEPT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5787n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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