A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624544



Internal ID6664708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110912099..110912969hg38UCSC Ensembl
Innerchr10:110912104..110912964hg38UCSC Ensembl
Outerchr10:110912094..110912974hg38UCSC Ensembl
chr10:112671857..112672727hg19UCSC Ensembl
Innerchr10:112671862..112672722hg19UCSC Ensembl
Outerchr10:112671852..112672732hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13935561, essv13935560
SamplesNA20894, NA21137
Known GenesBBIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624544
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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