A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623885



Internal ID6664052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78043176..78047146hg38UCSC Ensembl
Innerchr10:78043216..78047107hg38UCSC Ensembl
Outerchr10:78043137..78047186hg38UCSC Ensembl
chr10:79802934..79806904hg19UCSC Ensembl
Innerchr10:79802974..79806865hg19UCSC Ensembl
Outerchr10:79802895..79806944hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383971
hg193971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13866609
SamplesHG03054
Known GenesRPS24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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