A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756807



Internal ID3073705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37442414..37747570hg38UCSC Ensembl
chr10:37731342..38036498hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38305157
hg19305157
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622960
Supporting Variants
SamplesHG02697
Known GenesMTRNR2L7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756807
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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