A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6453918



Internal ID9066606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67263073..67263486hg38UCSC Ensembl
chr16:67296976..67297389hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668436
Supporting Variants
SamplesHG00734
Known GenesSLC9A5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6453918
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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