A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13823656



Internal ID3097888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56567518..56724586hg38UCSC Ensembl
Innerchr10:56567525..56724580hg38UCSC Ensembl
Outerchr10:56567512..56724593hg38UCSC Ensembl
chr10:58327278..58484346hg19UCSC Ensembl
Innerchr10:58327285..58484340hg19UCSC Ensembl
Outerchr10:58327272..58484353hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38157069
hg19157069
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623390
Supporting Variants
SamplesHG02722
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13823656
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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