A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756805



Internal ID3758621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37441894..37765337hg38UCSC Ensembl
Innerchr10:37441941..37765290hg38UCSC Ensembl
Outerchr10:37441847..37765384hg38UCSC Ensembl
chr10:37730822..38054265hg19UCSC Ensembl
Innerchr10:37730869..38054218hg19UCSC Ensembl
Outerchr10:37730775..38054312hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38323444
hg19323444
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622958
Supporting Variants
SamplesHG00473
Known GenesMTRNR2L7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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