A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624238



Internal ID6664405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93326745..93327875hg38UCSC Ensembl
Innerchr10:93326745..93327875hg38UCSC Ensembl
Outerchr10:93326352..93328181hg38UCSC Ensembl
chr10:95086502..95087632hg19UCSC Ensembl
Innerchr10:95086502..95087632hg19UCSC Ensembl
Outerchr10:95086109..95087938hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13899648, essv13899655, essv13899647, essv13899654, essv13899650, essv13899659, essv13899661, essv13899637, essv13899651, essv13899652, essv13899640, essv13899664, essv13899645, essv13899643, essv13899653, essv13899646, essv13899656, essv13899660, essv13899639, essv13899663, essv13899662, essv13899644, essv13899641, essv13899649, essv13899665, essv13899642, essv13899638, essv13899658, essv13899657
SamplesHG03163, NA19207, HG01079, NA19451, HG03571, HG02977, NA19834, HG02433, HG03376, HG01107, HG03520, HG03063, NA20291, HG03391, NA19384, HG03547, HG03168, HG01630, HG03157, NA19462, HG03132, HG02923, HG02645, HG03267, HG03078, NA19099, HG03123, HG02485, HG01890
Known GenesMYOF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624238
Frequency
Sample Size2504
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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