A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11746235



Internal ID6239394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186292802..186293580hg38UCSC Ensembl
Innerchr4:186292802..186293580hg38UCSC Ensembl
Outerchr4:186292375..186294044hg38UCSC Ensembl
chr4:187213956..187214734hg19UCSC Ensembl
Innerchr4:187213956..187214734hg19UCSC Ensembl
Outerchr4:187213529..187215198hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603526
Supporting Variants
SamplesNA19764
Known GenesF11-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11746235
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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