A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13682804



Internal ID1583614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4395503..4399198hg38UCSC Ensembl
Innerchr10:4395504..4399198hg38UCSC Ensembl
Outerchr10:4395503..4399199hg38UCSC Ensembl
chr10:4437695..4441390hg19UCSC Ensembl
Innerchr10:4437696..4441390hg19UCSC Ensembl
Outerchr10:4437695..4441391hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383696
hg193696
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622195
Supporting Variants
SamplesHG01464
Known GenesLINC00703
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13682804
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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