A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623827



Internal ID6663994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74292664..74293607hg38UCSC Ensembl
Innerchr10:74292664..74293607hg38UCSC Ensembl
Outerchr10:74292395..74293834hg38UCSC Ensembl
chr10:76052422..76053365hg19UCSC Ensembl
Innerchr10:76052422..76053365hg19UCSC Ensembl
Outerchr10:76052153..76053592hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863621, essv13863620
SamplesHG01051, HG00179
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623827
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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