A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623498



Internal ID7010354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62665876..62671111hg38UCSC Ensembl
Innerchr10:62665885..62671103hg38UCSC Ensembl
Outerchr10:62665868..62671120hg38UCSC Ensembl
chr10:64425636..64430871hg19UCSC Ensembl
Innerchr10:64425645..64430863hg19UCSC Ensembl
Outerchr10:64425628..64430880hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385236
hg195236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13833730, essv13833731, essv13833738, essv13833741, essv13833740, essv13833736, essv13833732, essv13833734, essv13833729, essv13833743, essv13833742, essv13833737, essv13833735, essv13833728, essv13833733, essv13833739
SamplesHG03548, HG03057, HG02318, NA19920, HG03069, HG03212, HG03511, NA19114, HG02256, HG02772, NA19834, HG01108, HG03084, HG03565, HG01377, HG02006
Known GenesZNF365
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623498
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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