A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13833458



Internal ID6616166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61957299..61963548hg38UCSC Ensembl
Innerchr10:61957331..61963516hg38UCSC Ensembl
Outerchr10:61957267..61963580hg38UCSC Ensembl
chr10:63717058..63723307hg19UCSC Ensembl
Innerchr10:63717090..63723275hg19UCSC Ensembl
Outerchr10:63717026..63723339hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg386250
hg196250
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623489
Supporting Variants
SamplesNA20783
Known GenesARID5B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13833458
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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