A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5928100



Internal ID8905503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72102314..72106292hg38UCSC Ensembl
Outerchr10:72102277..72106342hg38UCSC Ensembl
Innerchr10:73862072..73866050hg19UCSC Ensembl
Outerchr10:73862035..73866100hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384066
hg194066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673328
Supporting Variants
SamplesNA18909
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5928100
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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