A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935561



Internal ID3937377
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624544
Supporting Variants
SamplesNA21137
Known GenesBBIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935561
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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