A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15355157



Internal ID4404056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:238470..242038hg38UCSC Ensembl
Innerchr16:238970..241538hg38UCSC Ensembl
Outerchr16:237470..243038hg38UCSC Ensembl
chr16:288469..292037hg19UCSC Ensembl
Innerchr16:288969..291537hg19UCSC Ensembl
Outerchr16:287469..293037hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383569
hg193569
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637558
Supporting Variants
SamplesHG03920
Known GenesITFG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15355157
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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