A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13964288



Internal ID1100271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125710886..125717591hg38UCSC Ensembl
Innerchr10:125710886..125717591hg38UCSC Ensembl
Outerchr10:125710749..125717772hg38UCSC Ensembl
chr10:127399455..127406160hg19UCSC Ensembl
Innerchr10:127399455..127406160hg19UCSC Ensembl
Outerchr10:127399318..127406341hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386706
hg196706
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624842
Supporting Variants
SamplesHG00732
Known GenesFLJ37035
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13964288
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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