A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756806



Internal ID3758622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37442414..37747570hg38UCSC Ensembl
chr10:37731342..38036498hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38305157
hg19305157
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622959
Supporting Variants
SamplesHG00473
Known GenesMTRNR2L7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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