A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13896518



Internal ID3898334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91978631..91979564hg38UCSC Ensembl
Innerchr10:91978664..91979532hg38UCSC Ensembl
Outerchr10:91978599..91979597hg38UCSC Ensembl
chr10:93738388..93739321hg19UCSC Ensembl
Innerchr10:93738421..93739289hg19UCSC Ensembl
Outerchr10:93738356..93739354hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624215
Supporting Variants
SamplesHG01767
Known GenesBTAF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13896518
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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