A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13745715



Internal ID3093399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30524950..30547058hg38UCSC Ensembl
Innerchr10:30525450..30546558hg38UCSC Ensembl
Outerchr10:30523950..30548058hg38UCSC Ensembl
chr10:30813879..30835987hg19UCSC Ensembl
Innerchr10:30814379..30835487hg19UCSC Ensembl
Outerchr10:30812879..30836987hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3822109
hg1922109
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622791
Supporting Variants
SamplesHG02721
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13745715
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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