A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13729676



Internal ID3731492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26710076..26713214hg38UCSC Ensembl
Innerchr10:26710226..26713064hg38UCSC Ensembl
Outerchr10:26709926..26713364hg38UCSC Ensembl
chr10:26999005..27002143hg19UCSC Ensembl
Innerchr10:26999155..27001993hg19UCSC Ensembl
Outerchr10:26998855..27002293hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383139
hg193139
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622697
Supporting Variants
SamplesHG00329
Known GenesPDSS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13729676
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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