A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624702



Internal ID7011552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119305715..119308404hg38UCSC Ensembl
Innerchr10:119305715..119308404hg38UCSC Ensembl
Outerchr10:119305444..119308745hg38UCSC Ensembl
chr10:121065227..121067916hg19UCSC Ensembl
Innerchr10:121065227..121067916hg19UCSC Ensembl
Outerchr10:121064956..121068257hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382690
hg192690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946955, essv13946954, essv13946962, essv13946965, essv13946957, essv13946958, essv13946953, essv13946959, essv13946960, essv13946963, essv13946964, essv13946956, essv13946961
SamplesHG03484, HG03082, HG02811, HG02645, HG02489, NA19317, HG03369, HG02820, HG02307, NA19435, NA19467, NA19468, NA19346
Known GenesGRK5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624702
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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