A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865391



Internal ID13317742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86686808..86686821hg38UCSC Ensembl
Innerchr10:86686810..86686819hg38UCSC Ensembl
Outerchr10:86686806..86686823hg38UCSC Ensembl
chr10:88446565..88446578hg19UCSC Ensembl
Innerchr10:88446567..88446576hg19UCSC Ensembl
Outerchr10:88446563..88446580hg19UCSC Ensembl
chr10:88436545..88436558hg18UCSC Ensembl
Innerchr10:88436547..88436556hg18UCSC Ensembl
Outerchr10:88436543..88436560hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3354472
Supporting Variants
SamplesNA12005
Known GenesLDB3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865391
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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