A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13905689



Internal ID3907505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97075279..97077338hg38UCSC Ensembl
Innerchr10:97075279..97077338hg38UCSC Ensembl
Outerchr10:97075002..97077638hg38UCSC Ensembl
chr10:98835036..98837095hg19UCSC Ensembl
Innerchr10:98835036..98837095hg19UCSC Ensembl
Outerchr10:98834759..98837395hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382060
hg192060
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624309
Supporting Variants
SamplesHG02032
Known GenesSLIT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13905689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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