A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191921



Internal ID1193737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155877679..155897813hg38UCSC Ensembl
Innerchr3:155877679..155897813hg38UCSC Ensembl
Outerchr3:155877573..155897911hg38UCSC Ensembl
chr3:155595468..155615602hg19UCSC Ensembl
Innerchr3:155595468..155615602hg19UCSC Ensembl
Outerchr3:155595362..155615700hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3820135
hg1920135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598287
Supporting Variants
SamplesHG03642
Known GenesGMPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191921
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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