A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6175637



Internal ID9083932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65088834..65090601hg38UCSC Ensembl
chr14:65555552..65557319hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381768
hg191768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673460
Supporting Variants
SamplesHG01061
Known GenesLOC100506321, MAX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6175637
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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