A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863618



Internal ID3865434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74175523..74208165hg38UCSC Ensembl
Innerchr10:74175523..74208165hg38UCSC Ensembl
Outerchr10:74175023..74208665hg38UCSC Ensembl
chr10:75935281..75967923hg19UCSC Ensembl
Innerchr10:75935281..75967923hg19UCSC Ensembl
Outerchr10:75934781..75968423hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3832643
hg1932643
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623825
Supporting Variants
SamplesHG01069
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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