A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863622



Internal ID3865438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74349962..74357530hg38UCSC Ensembl
Innerchr10:74349995..74357497hg38UCSC Ensembl
Outerchr10:74349929..74357563hg38UCSC Ensembl
chr10:76109720..76117288hg19UCSC Ensembl
Innerchr10:76109753..76117255hg19UCSC Ensembl
Outerchr10:76109687..76117321hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg387569
hg197569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623828
Supporting Variants
SamplesNA19658
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863622
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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