A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13880321



Internal ID2489351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83904262..83905933hg38UCSC Ensembl
Innerchr10:83904287..83905908hg38UCSC Ensembl
Outerchr10:83904237..83905958hg38UCSC Ensembl
chr10:85664018..85665689hg19UCSC Ensembl
Innerchr10:85664043..85665664hg19UCSC Ensembl
Outerchr10:85663993..85665714hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381672
hg191672
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624026
Supporting Variants
SamplesHG02188
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13880321
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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