A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6374142



Internal ID9622562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64041509..64081808hg38UCSC Ensembl
Outerchr16:64041352..64081961hg38UCSC Ensembl
Innerchr16:64075413..64115712hg19UCSC Ensembl
Outerchr16:64075256..64115865hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840610
hg1940610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677592
Supporting Variants
SamplesNA19332
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6374142
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer