A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623825



Internal ID6663992
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863618
SamplesHG01069
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623825
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer