A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13695955



Internal ID5969754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10614095..10619059hg38UCSC Ensembl
Innerchr10:10614096..10619058hg38UCSC Ensembl
Outerchr10:10614094..10619060hg38UCSC Ensembl
chr10:10656058..10661022hg19UCSC Ensembl
Innerchr10:10656059..10661021hg19UCSC Ensembl
Outerchr10:10656057..10661023hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384965
hg194965
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622330
Supporting Variants
SamplesNA19380
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13695955
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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