A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622402



Internal ID7009261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13399754..13405464hg38UCSC Ensembl
Innerchr10:13399822..13405396hg38UCSC Ensembl
Outerchr10:13399686..13405532hg38UCSC Ensembl
chr10:13441754..13447464hg19UCSC Ensembl
Innerchr10:13441822..13447396hg19UCSC Ensembl
Outerchr10:13441686..13447532hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385711
hg195711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700171
SamplesNA18557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622402
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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