A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5660785



Internal ID9358477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30432373..30432895hg38UCSC Ensembl
Outerchr10:30432336..30432945hg38UCSC Ensembl
Innerchr10:30721302..30721824hg19UCSC Ensembl
Outerchr10:30721265..30721874hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665294
Supporting Variants
SamplesNA18553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5660785
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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