A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6586181



Internal ID9648119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12850975..12852263hg38UCSC Ensembl
Outerchr10:12850790..12852466hg38UCSC Ensembl
Innerchr10:12892975..12894263hg19UCSC Ensembl
Outerchr10:12892790..12894466hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656883
Supporting Variants
SamplesNA19380
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6586181
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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