A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624351



Internal ID7011207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99685955..99687349hg38UCSC Ensembl
Innerchr10:99685955..99687349hg38UCSC Ensembl
Outerchr10:99685728..99687523hg38UCSC Ensembl
chr10:101445712..101447106hg19UCSC Ensembl
Innerchr10:101445712..101447106hg19UCSC Ensembl
Outerchr10:101445485..101447280hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912280, essv13912271, essv13912277, essv13912274, essv13912272, essv13912281, essv13912278, essv13912279, essv13912283, essv13912282, essv13912270, essv13912275, essv13912276, essv13912273
SamplesHG02610, NA19092, HG03280, NA18916, NA18516, HG02976, HG03472, NA19449, NA18517, HG02546, HG03442, NA19713, NA19185, NA19346
Known GenesENTPD7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624351
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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