A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13896994



Internal ID1496453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92374675..92378009hg38UCSC Ensembl
Innerchr10:92375175..92377509hg38UCSC Ensembl
Outerchr10:92373675..92379009hg38UCSC Ensembl
chr10:94134432..94137766hg19UCSC Ensembl
Innerchr10:94134932..94137266hg19UCSC Ensembl
Outerchr10:94133432..94138766hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383335
hg193335
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624222
Supporting Variants
SamplesHG01375
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13896994
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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