A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10001851



Internal ID3667
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3586674
Supporting Variants
SamplesHG02699
Known GenesLPAR3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10001851
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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