A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13957463



Internal ID4417037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122791126..122797337hg38UCSC Ensembl
Innerchr10:122791126..122797337hg38UCSC Ensembl
Outerchr10:122790914..122797459hg38UCSC Ensembl
chr10:124550642..124556853hg19UCSC Ensembl
Innerchr10:124550642..124556853hg19UCSC Ensembl
Outerchr10:124550430..124556975hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386212
hg196212
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624787
Supporting Variants
SamplesHG03931
Known GenesFLJ46361
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13957463
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer