A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622344



Internal ID7009203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11711951..11713289hg38UCSC Ensembl
Innerchr10:11711970..11713270hg38UCSC Ensembl
Outerchr10:11711932..11713308hg38UCSC Ensembl
chr10:11753950..11755288hg19UCSC Ensembl
Innerchr10:11753969..11755269hg19UCSC Ensembl
Outerchr10:11753931..11755307hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381339
hg191339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13695997, essv13695996
SamplesHG04018, NA19149
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622344
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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