A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865418



Internal ID13317778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119864536..119864550hg38UCSC Ensembl
Innerchr10:119864538..119864548hg38UCSC Ensembl
Outerchr10:119864534..119864552hg38UCSC Ensembl
chr10:121624048..121624062hg19UCSC Ensembl
Innerchr10:121624050..121624060hg19UCSC Ensembl
Outerchr10:121624046..121624064hg19UCSC Ensembl
chr10:121614038..121614052hg18UCSC Ensembl
Innerchr10:121614040..121614050hg18UCSC Ensembl
Outerchr10:121614036..121614054hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3344248
Supporting Variants
SamplesNA12005
Known GenesMCMBP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865418
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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