A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13752102



Internal ID3753918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34690807..34696325hg38UCSC Ensembl
Innerchr10:34690838..34696295hg38UCSC Ensembl
Outerchr10:34690777..34696356hg38UCSC Ensembl
chr10:34979735..34985253hg19UCSC Ensembl
Innerchr10:34979766..34985223hg19UCSC Ensembl
Outerchr10:34979705..34985284hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385519
hg195519
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622877
Supporting Variants
SamplesHG01896
Known GenesPARD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13752102
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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