A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6084281



Internal ID9061684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50323190..50323493hg38UCSC Ensembl
chr10:52082950..52083253hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665424
Supporting Variants
SamplesHG00126
Known GenesSGMS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6084281
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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