A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6592748



Internal ID9395523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:26372197..26376917hg38UCSC Ensembl
Outerchr16:26372160..26376967hg38UCSC Ensembl
Innerchr16:26383518..26388238hg19UCSC Ensembl
Outerchr16:26383481..26388288hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384808
hg194808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675795
Supporting Variants
SamplesNA18599
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6592748
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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