A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010854



Internal ID6722945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75558807..75558886hg38UCSC Ensembl
chr17:73554888..73554967hg19UCSC Ensembl
chr17:71066483..71066562hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3880
hg1980
hg1880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3583616
SamplesHuRef
Known GenesLLGL2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010854
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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