A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678641



Internal ID9598060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88495558..88499016hg38UCSC Ensembl
chr16:88561966..88565424hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383459
hg193459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6472309
SamplesNA19079
Known GenesZFPM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678641
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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