A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11710119



Internal ID942998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174556104..174585923hg38UCSC Ensembl
Innerchr4:174556163..174585865hg38UCSC Ensembl
Outerchr4:174556046..174585982hg38UCSC Ensembl
chr4:175477255..175507074hg19UCSC Ensembl
Innerchr4:175477314..175507016hg19UCSC Ensembl
Outerchr4:175477197..175507133hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3829820
hg1929820
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603231
Supporting Variants
SamplesHG00566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11710119
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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