A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15702877



Internal ID6369898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55386020..55388057hg38UCSC Ensembl
Innerchr17:55386021..55388057hg38UCSC Ensembl
Outerchr17:55386020..55388058hg38UCSC Ensembl
chr17:53463381..53465418hg19UCSC Ensembl
Innerchr17:53463382..53465418hg19UCSC Ensembl
Outerchr17:53463381..53465419hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg382038
hg192038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640839
Supporting Variants
SamplesNA20299
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15702877
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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