A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5807581



Internal ID9133869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16670413..16683901hg38UCSC Ensembl
Outerchr17:16670256..16684054hg38UCSC Ensembl
Innerchr17:16573727..16587215hg19UCSC Ensembl
Outerchr17:16573570..16587368hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3813799
hg1913799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658786
Supporting Variants
SamplesHG01173
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5807581
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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