A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623019



Internal ID6663187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42606542..42612749hg38UCSC Ensembl
Innerchr10:42606542..42612749hg38UCSC Ensembl
Outerchr10:42606436..42612826hg38UCSC Ensembl
chr10:43101990..43108197hg19UCSC Ensembl
Innerchr10:43101990..43108197hg19UCSC Ensembl
Outerchr10:43101884..43108274hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386208
hg196208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764063, essv13764064
SamplesNA19390, NA18620
Known GenesZNF33B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623019
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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