A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623491



Internal ID7010347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62064458..62065845hg38UCSC Ensembl
Innerchr10:62064458..62065845hg38UCSC Ensembl
Outerchr10:62064332..62065992hg38UCSC Ensembl
chr10:63824217..63825604hg19UCSC Ensembl
Innerchr10:63824217..63825604hg19UCSC Ensembl
Outerchr10:63824091..63825751hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13833460, essv13833462, essv13833465, essv13833466, essv13833461, essv13833463, essv13833464
SamplesNA19028, NA19471, NA19338, HG01896, HG03565, HG03072, HG02808
Known GenesARID5B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623491
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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