A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13883020



Internal ID4394727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86111693..86115778hg38UCSC Ensembl
Innerchr10:86111726..86115746hg38UCSC Ensembl
Outerchr10:86111661..86115811hg38UCSC Ensembl
chr10:87871450..87875535hg19UCSC Ensembl
Innerchr10:87871483..87875503hg19UCSC Ensembl
Outerchr10:87871418..87875568hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624082
Supporting Variants
SamplesHG03914
Known GenesGRID1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13883020
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