A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15610340



Internal ID901922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9522493..9530103hg38UCSC Ensembl
Innerchr17:9522643..9529953hg38UCSC Ensembl
Outerchr17:9522343..9530253hg38UCSC Ensembl
chr17:9425810..9433420hg19UCSC Ensembl
Innerchr17:9425960..9433270hg19UCSC Ensembl
Outerchr17:9425660..9433570hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387611
hg197611
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639916
Supporting Variants
SamplesHG00525
Known GenesSTX8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15610340
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