A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13884184



Internal ID698369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87222342..87359039hg38UCSC Ensembl
Innerchr10:87222842..87358539hg38UCSC Ensembl
Outerchr10:87221342..87360039hg38UCSC Ensembl
chr10:88982099..89118796hg19UCSC Ensembl
Innerchr10:88982599..89118296hg19UCSC Ensembl
Outerchr10:88981099..89119796hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38136698
hg19136698
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624105
Supporting Variants
SamplesHG00328
Known GenesLOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13884184
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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