A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191924



Internal ID1193740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155933984..156058489hg38UCSC Ensembl
Innerchr3:155933984..156058489hg38UCSC Ensembl
Outerchr3:155933484..156058989hg38UCSC Ensembl
chr3:155651773..155776278hg19UCSC Ensembl
Innerchr3:155651773..155776278hg19UCSC Ensembl
Outerchr3:155651273..155776778hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38124506
hg19124506
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598289
Supporting Variants
SamplesNA21088
Known GenesGMPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191924
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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