A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15577692



Internal ID5920727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:898383..898997hg38UCSC Ensembl
Innerchr17:898383..898997hg38UCSC Ensembl
Outerchr17:897848..899494hg38UCSC Ensembl
chr17:801623..802237hg19UCSC Ensembl
Innerchr17:801623..802237hg19UCSC Ensembl
Outerchr17:801088..802734hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639651
Supporting Variants
SamplesNA19331
Known GenesNXN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15577692
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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