A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623032



Internal ID7009889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42888799..42892128hg38UCSC Ensembl
Innerchr10:42888826..42892102hg38UCSC Ensembl
Outerchr10:42888773..42892155hg38UCSC Ensembl
chr10:43384247..43387576hg19UCSC Ensembl
Innerchr10:43384274..43387550hg19UCSC Ensembl
Outerchr10:43384221..43387603hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383330
hg193330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764217, essv13764219, essv13764216, essv13764220, essv13764218
SamplesHG01947, NA19374, NA18867, HG03048, HG03049
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623032
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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