A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13833189



Internal ID2470805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60607009..60614874hg38UCSC Ensembl
Innerchr10:60607061..60614823hg38UCSC Ensembl
Outerchr10:60606958..60614926hg38UCSC Ensembl
chr10:62366767..62374632hg19UCSC Ensembl
Innerchr10:62366819..62374581hg19UCSC Ensembl
Outerchr10:62366716..62374684hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg387866
hg197866
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623470
Supporting Variants
SamplesHG02180
Known GenesANK3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13833189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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