A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6418154



Internal ID9395557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16751392..16753743hg38UCSC Ensembl
Outerchr2:16751358..16753778hg38UCSC Ensembl
Innerchr2:16932659..16935010hg19UCSC Ensembl
Outerchr2:16932625..16935045hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672666
Supporting Variants
SamplesNA19703
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6418154
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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