A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191923



Internal ID6851914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155897578..155981844hg38UCSC Ensembl
chr3:155615367..155699633hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3884267
hg1984267
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598288
Supporting Variants
SamplesNA21088
Known GenesGMPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191923
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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