A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6248722



Internal ID9901624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:898386..898997hg38UCSC Ensembl
chr17:801626..802237hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675496
Supporting Variants
SamplesNA20796
Known GenesNXN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6248722
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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