A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624908



Internal ID7011758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128784082..128787325hg38UCSC Ensembl
Innerchr10:128784095..128787312hg38UCSC Ensembl
Outerchr10:128784069..128787338hg38UCSC Ensembl
chr10:130582346..130585589hg19UCSC Ensembl
Innerchr10:130582359..130585576hg19UCSC Ensembl
Outerchr10:130582333..130585602hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383244
hg193244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13971751, essv13971750
SamplesNA18520, HG01086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624908
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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