A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657427



Internal ID9923532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23498296..23503322hg38UCSC Ensembl
Outerchr16:23498259..23503372hg38UCSC Ensembl
Innerchr16:23509617..23514643hg19UCSC Ensembl
Outerchr16:23509580..23514693hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg385114
hg195114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv485e199
Supporting Variantsessv6410410
SamplesHG00125
Known GenesGGA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657427
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