A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13689297



Internal ID5193485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7461159..7535400hg38UCSC Ensembl
Innerchr10:7461184..7535375hg38UCSC Ensembl
Outerchr10:7461134..7535425hg38UCSC Ensembl
chr10:7503121..7577362hg19UCSC Ensembl
Innerchr10:7503146..7577337hg19UCSC Ensembl
Outerchr10:7503096..7577387hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3874242
hg1974242
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622270
Supporting Variants
SamplesNA18611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13689297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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