A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13896517



Internal ID2719251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91911759..91919243hg38UCSC Ensembl
Innerchr10:91911759..91919243hg38UCSC Ensembl
Outerchr10:91911521..91919488hg38UCSC Ensembl
chr10:93671516..93679000hg19UCSC Ensembl
Innerchr10:93671516..93679000hg19UCSC Ensembl
Outerchr10:93671278..93679245hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg387485
hg197485
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624214
Supporting Variants
SamplesHG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13896517
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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