A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15661280



Internal ID2202981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33572945..33576610hg38UCSC Ensembl
Innerchr17:33572945..33576610hg38UCSC Ensembl
Outerchr17:33572717..33576852hg38UCSC Ensembl
chr17:31899964..31903629hg19UCSC Ensembl
Innerchr17:31899964..31903629hg19UCSC Ensembl
Outerchr17:31899736..31903871hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640409
Supporting Variants
SamplesHG01985
Known GenesASIC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15661280
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer