A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13883957



Internal ID5314815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86488139..86493197hg38UCSC Ensembl
Innerchr10:86488163..86493174hg38UCSC Ensembl
Outerchr10:86488116..86493221hg38UCSC Ensembl
chr10:88247896..88252954hg19UCSC Ensembl
Innerchr10:88247920..88252931hg19UCSC Ensembl
Outerchr10:88247873..88252978hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624091
Supporting Variants
SamplesNA18864
Known GenesWAPAL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13883957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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