A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15657013



Internal ID3408918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29350329..29354208hg38UCSC Ensembl
Innerchr17:29350829..29353708hg38UCSC Ensembl
Outerchr17:29349329..29355208hg38UCSC Ensembl
chr17:27677347..27681226hg19UCSC Ensembl
Innerchr17:27677847..27680726hg19UCSC Ensembl
Outerchr17:27676347..27682226hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383880
hg193880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640325
Supporting Variants
SamplesHG03054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15657013
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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