A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624219



Internal ID7011075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92319897..92323014hg38UCSC Ensembl
Innerchr10:92319974..92322940hg38UCSC Ensembl
Outerchr10:92319654..92323257hg38UCSC Ensembl
chr10:94079654..94082771hg19UCSC Ensembl
Innerchr10:94079731..94082697hg19UCSC Ensembl
Outerchr10:94079411..94083014hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13896537, essv13896535, essv13896528, essv13896522, essv13896536, essv13896543, essv13896524, essv13896538, essv13896540, essv13896526, essv13896523, essv13896529, essv13896541, essv13896532, essv13896527, essv13896539, essv13896542, essv13896531, essv13896530, essv13896533, essv13896525, essv13896534
SamplesHG03096, NA19350, HG01305, HG02769, NA19374, NA19384, NA19041, HG02703, HG02315, NA20342, NA19451, HG03061, HG03088, HG01882, HG03428, HG02953, HG02585, HG02330, HG02983, NA19467, NA19351, NA19431
Known GenesMARCH5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624219
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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