A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5537243



Internal ID9163154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13719668..13724026hg38UCSC Ensembl
Outerchr17:13719606..13724092hg38UCSC Ensembl
Innerchr17:13622985..13627343hg19UCSC Ensembl
Outerchr17:13622923..13627409hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384487
hg194487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673672
Supporting Variants
SamplesHG01359
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5537243
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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