A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5761262



Internal ID9608002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055626..91055947hg38UCSC Ensembl
chr10:92815383..92815704hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658309
Supporting Variants
SamplesNA19257
Known GenesLINC00502
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5761262
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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