A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6356767



Internal ID9334170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87842599..87844425hg38UCSC Ensembl
Outerchr16:87842562..87844475hg38UCSC Ensembl
Innerchr16:87876205..87878031hg19UCSC Ensembl
Outerchr16:87876168..87878081hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381914
hg191914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668850
Supporting Variants
SamplesHG00610
Known GenesSLC7A5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6356767
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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