A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13688330



Internal ID4521393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6837772..6861917hg38UCSC Ensembl
Innerchr10:6837772..6861917hg38UCSC Ensembl
Outerchr10:6837272..6862417hg38UCSC Ensembl
chr10:6879734..6903879hg19UCSC Ensembl
Innerchr10:6879734..6903879hg19UCSC Ensembl
Outerchr10:6879234..6904379hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3824146
hg1924146
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622257
Supporting Variants
SamplesHG04019
Known GenesLINC00707
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13688330
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