A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13753908



Internal ID972630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35928636..35931769hg38UCSC Ensembl
Innerchr10:35928636..35931769hg38UCSC Ensembl
Outerchr10:35928136..35932269hg38UCSC Ensembl
chr10:36217564..36220697hg19UCSC Ensembl
Innerchr10:36217564..36220697hg19UCSC Ensembl
Outerchr10:36217064..36221197hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383134
hg193134
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622909
Supporting Variants
SamplesHG00599
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13753908
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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