A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623790



Internal ID6663957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72075171..72085218hg38UCSC Ensembl
Innerchr10:72075171..72085218hg38UCSC Ensembl
Outerchr10:72074990..72085448hg38UCSC Ensembl
chr10:73834929..73844976hg19UCSC Ensembl
Innerchr10:73834929..73844976hg19UCSC Ensembl
Outerchr10:73834748..73845206hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810048
hg1910048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861554
SamplesNA20854
Known GenesSPOCK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623790
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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