A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624848



Internal ID7011698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126025003..126025643hg38UCSC Ensembl
Innerchr10:126025022..126025624hg38UCSC Ensembl
Outerchr10:126024984..126025662hg38UCSC Ensembl
chr10:127713572..127714212hg19UCSC Ensembl
Innerchr10:127713591..127714193hg19UCSC Ensembl
Outerchr10:127713553..127714231hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13964374
SamplesHG03124
Known GenesADAM12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624848
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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