A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586674



Internal ID6626984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84845234..84845932hg38UCSC Ensembl
Innerchr1:84845251..84845915hg38UCSC Ensembl
Outerchr1:84845217..84845949hg38UCSC Ensembl
chr1:85310917..85311615hg19UCSC Ensembl
Innerchr1:85310934..85311598hg19UCSC Ensembl
Outerchr1:85310900..85311632hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10001851, essv10001852
SamplesHG02699, HG02700
Known GenesLPAR3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586674
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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