A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890047



Internal ID3891863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88489037..88688695hg38UCSC Ensembl
chr10:90248794..90448452hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38199659
hg19199659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624131
Supporting Variants
SamplesHG02790
Known GenesLIPF, LIPJ, RNLS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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