A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5865181



Internal ID9069885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45837756..45838143hg38UCSC Ensembl
Outerchr17:45837719..45838193hg38UCSC Ensembl
Innerchr17:43915122..43915509hg19UCSC Ensembl
Outerchr17:43915085..43915559hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673017
Supporting Variants
SamplesHG00737
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5865181
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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