A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659592



Internal ID9579011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88495889..88498187hg38UCSC Ensembl
Outerchr16:88495855..88498222hg38UCSC Ensembl
Innerchr16:88562297..88564595hg19UCSC Ensembl
Outerchr16:88562263..88564630hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382368
hg192368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv516e199
Supporting Variantsessv5838972
SamplesNA18907
Known GenesZFPM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659592
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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