A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623093



Internal ID6663261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45486664..45500662hg38UCSC Ensembl
Innerchr10:45486664..45500662hg38UCSC Ensembl
Outerchr10:45486164..45501162hg38UCSC Ensembl
chr10:45982112..45996110hg19UCSC Ensembl
Innerchr10:45982112..45996110hg19UCSC Ensembl
Outerchr10:45981612..45996610hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813999
hg1913999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13770335
SamplesHG03380
Known GenesMARCH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623093
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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