A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13875562



Internal ID5062617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81876350..81877417hg38UCSC Ensembl
Innerchr10:81876376..81877391hg38UCSC Ensembl
Outerchr10:81876324..81877443hg38UCSC Ensembl
chr10:83636106..83637173hg19UCSC Ensembl
Innerchr10:83636132..83637147hg19UCSC Ensembl
Outerchr10:83636080..83637199hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623983
Supporting Variants
SamplesNA18536
Known GenesNRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13875562
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