A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677045



Internal ID9943150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59729082..59766549hg38UCSC Ensembl
chr10:61488840..61526307hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3837468
hg1937468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5704590, essv6305831, essv6569266, essv6536663, essv6490006, essv5950884, essv6020085, essv6160307, essv5428224
SamplesHG00143, NA12348, NA11932, NA19901, NA11831, NA20787, HG00331, NA12046, NA06986
Known GenesLINC00948
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677045
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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