A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671736



Internal ID9591155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85032526..85054494hg38UCSC Ensembl
Outerchr16:85032369..85054647hg38UCSC Ensembl
Innerchr16:85066132..85088100hg19UCSC Ensembl
Outerchr16:85065975..85088253hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822279
hg1922279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6507856
SamplesHG00421
Known GenesKIAA0513
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671736
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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