A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622260



Internal ID7009119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6935011..6945541hg38UCSC Ensembl
Innerchr10:6935018..6945535hg38UCSC Ensembl
Outerchr10:6935005..6945548hg38UCSC Ensembl
chr10:6976973..6987503hg19UCSC Ensembl
Innerchr10:6976980..6987497hg19UCSC Ensembl
Outerchr10:6976967..6987510hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810531
hg1910531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13688339, essv13688340, essv13688338
SamplesHG00309, NA18975, HG00436
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622260
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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